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Nikki co-chairs the firm's Government Matters \u0026amp; Regulatory practice management group, which is comprised of 200+ lawyers and consultants in eight practice areas.\u0026nbsp; Nikki previously co-chaired\u0026nbsp;the firm\u0026rsquo;s Life Sciences and Healthcare Industry Group for six years, which is comprised of more than 450\u0026nbsp;lawyers across seventeen practice areas in the firm.\u0026nbsp; In 2024, Nikki was a winner of Corporate Counsel's 2024 Women, Influence \u0026amp; Power in Law Award for Law Firm Thought Leadership.\u0026nbsp; Nikki is ranked nationally by \u003cem\u003eChambers USA\u003c/em\u003e\u0026nbsp;for Life Sciences: Regulatory Compliance and for Pharmaceuticals/Medical Products Regulatory from 2021-2025, named a\u0026nbsp;\u003cem\u003eLMG Life Sciences Star\u003c/em\u003e in FDA Pharmaceutical and in FDA Medical Device from 2019-2025, and was named a\u0026nbsp;\u003cem\u003eLaw360 Compliance MVP\u003c/em\u003e\u0026nbsp;in 2020.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eAs Deputy Chair of our FDA \u0026amp; Life Sciences practice, Nikki advises pharmaceutical and medical device companies on pre- and post-market FDA regulatory compliance and enforcement matters ranging from clinical trials, good manufacturing practices, to labeling, advertising, and promotion of FDA-regulated products.\u0026nbsp; Nikki has been the lead FDA regulatory advisor to her clients on 250+ transactional matters.\u0026nbsp; She conducts investigations into FDA clinical trials and post-marking noncompliance, acts as lead compliance and regulatory counsel for several companies under Corporate Integrity Agreements (CIAs) and has led several CMS Open Payments compliance audits.\u0026nbsp; She is an expert on federal Open Payments, state, and international transparency/disclosure laws and leads two pharma and device industry compliance coalitions.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eNikki counsels pharma and device companies on FDA inspections, Form 483s, Warning Letters, product recalls, import detentions, clinical holds, and other FDA compliance and enforcement matters.\u0026nbsp; She conducts risk assessments and internal investigations into allegations of FDA and healthcare program noncompliance.\u0026nbsp; She routinely advises company executives and board members and represents her clients before federal agencies.\u0026nbsp; She has established robust compliance programs and policies for numerous life sciences companies. Nikki has also served as an interim General Counsel and as a Chief Compliance Officer for her life sciences clients.\u003c/p\u003e\n\u003cp\u003eNikki leads two pharma and device industry coalitions on transparency and disclosure laws.\u0026nbsp; The\u0026nbsp;\u003cem\u003eAd Hoc Sunshine and State Law Compliance Group\u003c/em\u003e is a coalition she advises on federal Sunshine Act and state transparency/disclosure and gift ban laws.\u0026nbsp; The \u003cem\u003eInternational Marketing and Disclosure Compliance Group\u003c/em\u003e is a separate coalition of companies she advises on the growing area of transparency and disclosure laws and industry codes of conduct in the EU, Australia, Japan, and numerous other countries and regions.\u003c/p\u003e\n\u003cp\u003eKing \u0026amp; Spalding\u0026rsquo;s FDA \u0026amp; Life Sciences Practice has been named \u003cem\u003eLaw360\u003c/em\u003e Practice Group of the Year from 2017-2020.\u0026nbsp; King \u0026amp; Spalding\u0026rsquo;s FDA \u0026amp; Life Sciences Practice is ranked by Chambers Legal, LMG Life Sciences, U.S. News, and Best Lawyers.\u0026nbsp; According to\u0026nbsp;\u003cem\u003eChambers USA, sources praise Nikki as being \"thoughtful, quick to respond and available.\" -- Chambers USA\u003c/em\u003e\u0026nbsp;(2022)\u003c/p\u003e\n\u003cp\u003eNikki is a frequent speaker and author on FDA advertising/promotion, clinical trials, compliance, and transparency law matters.\u0026nbsp; Nikki was also selected to Law360's 2021 Compliance Editorial Advisory Board\u0026nbsp;and has served\u0026nbsp;on the\u0026nbsp;Advisory Board for FDAnews and the PCF Pharma Congress planning committee.\u0026nbsp; She was formerly on the Food and Drug Law Institute (FDLI) Editorial Advisory Board for the \u003cem\u003eFDLI Food \u0026amp; Drug Law Journal\u003c/em\u003e and a member of the FDLI Medical Device Committee.\u0026nbsp; Nikki has also served on the Leadership Advisory Board for the National Women\u0026rsquo;s Law Center and on the Special Gifts Committee for the Arlington Free Clinic for more than ten\u0026nbsp;years.\u003c/p\u003e\n\u003cp\u003eNikki was elected by her partners in 2017 to serve for three years\u0026nbsp;on the firm\u0026rsquo;s Policy Committee, which is the firm's executive management committee.\u0026nbsp; Nikki served for many years on the firm\u0026rsquo;s Lateral Partner Committee and on the firm's Partners Committee, and was also the Hiring Partner for the Washington, D.C. office.\u003c/p\u003e","slug":"nikki-reeves","email":"nreeves@kslaw.com","phone":null,"matters":["\u003cp\u003eAdvised companies on FDA advertising and promotion rules for drugs, devices, and cosmetics, including social media, new product launches, DTC, physician and payor communications, broadcast ads, reprints, and investor communications.\u003c/p\u003e","\u003cp\u003eAdvised on CMS Open Payments compliance audits and compliance with the federal Physician Payment Sunshine (Open Payments) law, state laws targeting industry marketing practices, sales representation licensing, drug price transparency, and disclosure of clinical trial data. Advised on compliance with global transparency laws and industry codes of conduct.\u003c/p\u003e","\u003cp\u003eAdvised life sciences clients on preparing for FDA inspections of clinical trials sites and manufacturing facilities, and responding to FDA Form 483s, FDA Warning Letters, product recalls, import detentions, and government investigations involving alleged advertising/promotion violations.\u003c/p\u003e","\u003cp\u003eConducted FDA regulatory due diligence and related counseling in connection with more than 200+ transactions involving pharmaceutical, medical device, biotechnology, and cosmetic companies.\u003c/p\u003e","\u003cp\u003eStand up healthcare compliance programs for pharmaceutical and medical device manufacturers and related healthcare compliance policies and codes of conduct. Served as interim Chief Compliance Officer for a pharmaceutical manufacturer for a two year period and managed all aspects of the company healthcare compliance program.\u003c/p\u003e","\u003cp\u003eConducted internal investigations into potential FDA GCP, GMP, and healthcare compliance policy violations.\u003c/p\u003e","\u003cp\u003eLed risk assessments of healthcare regulatory compliance programs and policies and advised on compliance with FDA regulations, HHS OIG Compliance Program Guidance, and the PhRMA and AdvaMed Codes on Interactions with Healthcare Professionals.\u003c/p\u003e"],"taggings":{"tags":[],"meta_tags":[{"id":245}]},"expertise":[{"id":81,"guid":"81.capabilities","index":0,"source":"capabilities"},{"id":761,"guid":"761.smart_tags","index":1,"source":"smartTags"},{"id":21,"guid":"21.capabilities","index":2,"source":"capabilities"},{"id":23,"guid":"23.capabilities","index":3,"source":"capabilities"},{"id":32,"guid":"32.capabilities","index":4,"source":"capabilities"},{"id":17,"guid":"17.capabilities","index":5,"source":"capabilities"},{"id":107,"guid":"107.capabilities","index":6,"source":"capabilities"},{"id":103,"guid":"103.capabilities","index":7,"source":"capabilities"},{"id":970,"guid":"970.smart_tags","index":8,"source":"smartTags"},{"id":109,"guid":"109.capabilities","index":9,"source":"capabilities"},{"id":112,"guid":"112.capabilities","index":10,"source":"capabilities"},{"id":114,"guid":"114.capabilities","index":11,"source":"capabilities"},{"id":120,"guid":"120.capabilities","index":12,"source":"capabilities"},{"id":122,"guid":"122.capabilities","index":13,"source":"capabilities"},{"id":1193,"guid":"1193.smart_tags","index":14,"source":"smartTags"},{"id":1223,"guid":"1223.smart_tags","index":15,"source":"smartTags"},{"id":135,"guid":"135.capabilities","index":16,"source":"capabilities"}],"is_active":true,"last_name":"Reeves","nick_name":"Nikki","clerkships":[],"first_name":"Nikki","title_rank":9999,"updated_by":202,"law_schools":[],"middle_name":" ","name_suffix":"","recognitions":[{"title":"Women, Influence \u0026 Power in Law Award for Thought Leadership","detail":"Corporate Counsel 2024"}],"linked_in_url":null,"seodescription":null,"primary_title_id":15,"translated_fields":{"en":{"bio":"\u003cp\u003eNikki Reeves is an FDA and healthcare regulatory compliance lawyer with more than 25\u0026nbsp;years of experience.\u0026nbsp; Nikki co-chairs the firm's Government Matters \u0026amp; Regulatory practice management group, which is comprised of 200+ lawyers and consultants in eight practice areas.\u0026nbsp; Nikki previously co-chaired\u0026nbsp;the firm\u0026rsquo;s Life Sciences and Healthcare Industry Group for six years, which is comprised of more than 450\u0026nbsp;lawyers across seventeen practice areas in the firm.\u0026nbsp; In 2024, Nikki was a winner of Corporate Counsel's 2024 Women, Influence \u0026amp; Power in Law Award for Law Firm Thought Leadership.\u0026nbsp; Nikki is ranked nationally by \u003cem\u003eChambers USA\u003c/em\u003e\u0026nbsp;for Life Sciences: Regulatory Compliance and for Pharmaceuticals/Medical Products Regulatory from 2021-2025, named a\u0026nbsp;\u003cem\u003eLMG Life Sciences Star\u003c/em\u003e in FDA Pharmaceutical and in FDA Medical Device from 2019-2025, and was named a\u0026nbsp;\u003cem\u003eLaw360 Compliance MVP\u003c/em\u003e\u0026nbsp;in 2020.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eAs Deputy Chair of our FDA \u0026amp; Life Sciences practice, Nikki advises pharmaceutical and medical device companies on pre- and post-market FDA regulatory compliance and enforcement matters ranging from clinical trials, good manufacturing practices, to labeling, advertising, and promotion of FDA-regulated products.\u0026nbsp; Nikki has been the lead FDA regulatory advisor to her clients on 250+ transactional matters.\u0026nbsp; She conducts investigations into FDA clinical trials and post-marking noncompliance, acts as lead compliance and regulatory counsel for several companies under Corporate Integrity Agreements (CIAs) and has led several CMS Open Payments compliance audits.\u0026nbsp; She is an expert on federal Open Payments, state, and international transparency/disclosure laws and leads two pharma and device industry compliance coalitions.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eNikki counsels pharma and device companies on FDA inspections, Form 483s, Warning Letters, product recalls, import detentions, clinical holds, and other FDA compliance and enforcement matters.\u0026nbsp; She conducts risk assessments and internal investigations into allegations of FDA and healthcare program noncompliance.\u0026nbsp; She routinely advises company executives and board members and represents her clients before federal agencies.\u0026nbsp; She has established robust compliance programs and policies for numerous life sciences companies. Nikki has also served as an interim General Counsel and as a Chief Compliance Officer for her life sciences clients.\u003c/p\u003e\n\u003cp\u003eNikki leads two pharma and device industry coalitions on transparency and disclosure laws.\u0026nbsp; The\u0026nbsp;\u003cem\u003eAd Hoc Sunshine and State Law Compliance Group\u003c/em\u003e is a coalition she advises on federal Sunshine Act and state transparency/disclosure and gift ban laws.\u0026nbsp; The \u003cem\u003eInternational Marketing and Disclosure Compliance Group\u003c/em\u003e is a separate coalition of companies she advises on the growing area of transparency and disclosure laws and industry codes of conduct in the EU, Australia, Japan, and numerous other countries and regions.\u003c/p\u003e\n\u003cp\u003eKing \u0026amp; Spalding\u0026rsquo;s FDA \u0026amp; Life Sciences Practice has been named \u003cem\u003eLaw360\u003c/em\u003e Practice Group of the Year from 2017-2020.\u0026nbsp; King \u0026amp; Spalding\u0026rsquo;s FDA \u0026amp; Life Sciences Practice is ranked by Chambers Legal, LMG Life Sciences, U.S. News, and Best Lawyers.\u0026nbsp; According to\u0026nbsp;\u003cem\u003eChambers USA, sources praise Nikki as being \"thoughtful, quick to respond and available.\" -- Chambers USA\u003c/em\u003e\u0026nbsp;(2022)\u003c/p\u003e\n\u003cp\u003eNikki is a frequent speaker and author on FDA advertising/promotion, clinical trials, compliance, and transparency law matters.\u0026nbsp; Nikki was also selected to Law360's 2021 Compliance Editorial Advisory Board\u0026nbsp;and has served\u0026nbsp;on the\u0026nbsp;Advisory Board for FDAnews and the PCF Pharma Congress planning committee.\u0026nbsp; She was formerly on the Food and Drug Law Institute (FDLI) Editorial Advisory Board for the \u003cem\u003eFDLI Food \u0026amp; Drug Law Journal\u003c/em\u003e and a member of the FDLI Medical Device Committee.\u0026nbsp; Nikki has also served on the Leadership Advisory Board for the National Women\u0026rsquo;s Law Center and on the Special Gifts Committee for the Arlington Free Clinic for more than ten\u0026nbsp;years.\u003c/p\u003e\n\u003cp\u003eNikki was elected by her partners in 2017 to serve for three years\u0026nbsp;on the firm\u0026rsquo;s Policy Committee, which is the firm's executive management committee.\u0026nbsp; Nikki served for many years on the firm\u0026rsquo;s Lateral Partner Committee and on the firm's Partners Committee, and was also the Hiring Partner for the Washington, D.C. office.\u003c/p\u003e","matters":["\u003cp\u003eAdvised companies on FDA advertising and promotion rules for drugs, devices, and cosmetics, including social media, new product launches, DTC, physician and payor communications, broadcast ads, reprints, and investor communications.\u003c/p\u003e","\u003cp\u003eAdvised on CMS Open Payments compliance audits and compliance with the federal Physician Payment Sunshine (Open Payments) law, state laws targeting industry marketing practices, sales representation licensing, drug price transparency, and disclosure of clinical trial data. Advised on compliance with global transparency laws and industry codes of conduct.\u003c/p\u003e","\u003cp\u003eAdvised life sciences clients on preparing for FDA inspections of clinical trials sites and manufacturing facilities, and responding to FDA Form 483s, FDA Warning Letters, product recalls, import detentions, and government investigations involving alleged advertising/promotion violations.\u003c/p\u003e","\u003cp\u003eConducted FDA regulatory due diligence and related counseling in connection with more than 200+ transactions involving pharmaceutical, medical device, biotechnology, and cosmetic companies.\u003c/p\u003e","\u003cp\u003eStand up healthcare compliance programs for pharmaceutical and medical device manufacturers and related healthcare compliance policies and codes of conduct. Served as interim Chief Compliance Officer for a pharmaceutical manufacturer for a two year period and managed all aspects of the company healthcare compliance program.\u003c/p\u003e","\u003cp\u003eConducted internal investigations into potential FDA GCP, GMP, and healthcare compliance policy violations.\u003c/p\u003e","\u003cp\u003eLed risk assessments of healthcare regulatory compliance programs and policies and advised on compliance with FDA regulations, HHS OIG Compliance Program Guidance, and the PhRMA and AdvaMed Codes on Interactions with Healthcare Professionals.\u003c/p\u003e"],"recognitions":[{"title":"Women, Influence \u0026 Power in Law Award for Thought Leadership","detail":"Corporate Counsel 2024"}]},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":1139}]},"capability_group_id":2},"created_at":"2025-07-29T16:08:40.000Z","updated_at":"2025-07-29T16:08:40.000Z","searchable_text":"Reeves{{ FIELD }}{:title=\u0026gt;\"Women, Influence \u0026amp; Power in Law Award for Thought Leadership\", :detail=\u0026gt;\"Corporate Counsel 2024\"}{{ FIELD }}Advised companies on FDA advertising and promotion rules for drugs, devices, and cosmetics, including social media, new product launches, DTC, physician and payor communications, broadcast ads, reprints, and investor communications.{{ FIELD }}Advised on CMS Open Payments compliance audits and compliance with the federal Physician Payment Sunshine (Open Payments) law, state laws targeting industry marketing practices, sales representation licensing, drug price transparency, and disclosure of clinical trial data. Advised on compliance with global transparency laws and industry codes of conduct.{{ FIELD }}Advised life sciences clients on preparing for FDA inspections of clinical trials sites and manufacturing facilities, and responding to FDA Form 483s, FDA Warning Letters, product recalls, import detentions, and government investigations involving alleged advertising/promotion violations.{{ FIELD }}Conducted FDA regulatory due diligence and related counseling in connection with more than 200+ transactions involving pharmaceutical, medical device, biotechnology, and cosmetic companies.{{ FIELD }}Stand up healthcare compliance programs for pharmaceutical and medical device manufacturers and related healthcare compliance policies and codes of conduct. Served as interim Chief Compliance Officer for a pharmaceutical manufacturer for a two year period and managed all aspects of the company healthcare compliance program.{{ FIELD }}Conducted internal investigations into potential FDA GCP, GMP, and healthcare compliance policy violations.{{ FIELD }}Led risk assessments of healthcare regulatory compliance programs and policies and advised on compliance with FDA regulations, HHS OIG Compliance Program Guidance, and the PhRMA and AdvaMed Codes on Interactions with Healthcare Professionals.{{ FIELD }}Nikki Reeves is an FDA and healthcare regulatory compliance lawyer with more than 25 years of experience.  Nikki co-chairs the firm's Government Matters \u0026amp; Regulatory practice management group, which is comprised of 200+ lawyers and consultants in eight practice areas.  Nikki previously co-chaired the firm’s Life Sciences and Healthcare Industry Group for six years, which is comprised of more than 450 lawyers across seventeen practice areas in the firm.  In 2024, Nikki was a winner of Corporate Counsel's 2024 Women, Influence \u0026amp; Power in Law Award for Law Firm Thought Leadership.  Nikki is ranked nationally by Chambers USA for Life Sciences: Regulatory Compliance and for Pharmaceuticals/Medical Products Regulatory from 2021-2025, named a LMG Life Sciences Star in FDA Pharmaceutical and in FDA Medical Device from 2019-2025, and was named a Law360 Compliance MVP in 2020. \nAs Deputy Chair of our FDA \u0026amp; Life Sciences practice, Nikki advises pharmaceutical and medical device companies on pre- and post-market FDA regulatory compliance and enforcement matters ranging from clinical trials, good manufacturing practices, to labeling, advertising, and promotion of FDA-regulated products.  Nikki has been the lead FDA regulatory advisor to her clients on 250+ transactional matters.  She conducts investigations into FDA clinical trials and post-marking noncompliance, acts as lead compliance and regulatory counsel for several companies under Corporate Integrity Agreements (CIAs) and has led several CMS Open Payments compliance audits.  She is an expert on federal Open Payments, state, and international transparency/disclosure laws and leads two pharma and device industry compliance coalitions. \nNikki counsels pharma and device companies on FDA inspections, Form 483s, Warning Letters, product recalls, import detentions, clinical holds, and other FDA compliance and enforcement matters.  She conducts risk assessments and internal investigations into allegations of FDA and healthcare program noncompliance.  She routinely advises company executives and board members and represents her clients before federal agencies.  She has established robust compliance programs and policies for numerous life sciences companies. Nikki has also served as an interim General Counsel and as a Chief Compliance Officer for her life sciences clients.\nNikki leads two pharma and device industry coalitions on transparency and disclosure laws.  The Ad Hoc Sunshine and State Law Compliance Group is a coalition she advises on federal Sunshine Act and state transparency/disclosure and gift ban laws.  The International Marketing and Disclosure Compliance Group is a separate coalition of companies she advises on the growing area of transparency and disclosure laws and industry codes of conduct in the EU, Australia, Japan, and numerous other countries and regions.\nKing \u0026amp; Spalding’s FDA \u0026amp; Life Sciences Practice has been named Law360 Practice Group of the Year from 2017-2020.  King \u0026amp; Spalding’s FDA \u0026amp; Life Sciences Practice is ranked by Chambers Legal, LMG Life Sciences, U.S. News, and Best Lawyers.  According to Chambers USA, sources praise Nikki as being \"thoughtful, quick to respond and available.\" -- Chambers USA (2022)\nNikki is a frequent speaker and author on FDA advertising/promotion, clinical trials, compliance, and transparency law matters.  Nikki was also selected to Law360's 2021 Compliance Editorial Advisory Board and has served on the Advisory Board for FDAnews and the PCF Pharma Congress planning committee.  She was formerly on the Food and Drug Law Institute (FDLI) Editorial Advisory Board for the FDLI Food \u0026amp; Drug Law Journal and a member of the FDLI Medical Device Committee.  Nikki has also served on the Leadership Advisory Board for the National Women’s Law Center and on the Special Gifts Committee for the Arlington Free Clinic for more than ten years.\nNikki was elected by her partners in 2017 to serve for three years on the firm’s Policy Committee, which is the firm's executive management committee.  Nikki served for many years on the firm’s Lateral Partner Committee and on the firm's Partners Committee, and was also the Hiring Partner for the Washington, D.C. office. Kelly Reeves Partner Women, Influence \u0026amp; Power in Law Award for Thought Leadership Corporate Counsel 2024 North Carolina State University  University of Maryland  North Carolina State University  District of Columbia Maryland Advised companies on FDA advertising and promotion rules for drugs, devices, and cosmetics, including social media, new product launches, DTC, physician and payor communications, broadcast ads, reprints, and investor communications. Advised on CMS Open Payments compliance audits and compliance with the federal Physician Payment Sunshine (Open Payments) law, state laws targeting industry marketing practices, sales representation licensing, drug price transparency, and disclosure of clinical trial data. Advised on compliance with global transparency laws and industry codes of conduct. Advised life sciences clients on preparing for FDA inspections of clinical trials sites and manufacturing facilities, and responding to FDA Form 483s, FDA Warning Letters, product recalls, import detentions, and government investigations involving alleged advertising/promotion violations. Conducted FDA regulatory due diligence and related counseling in connection with more than 200+ transactions involving pharmaceutical, medical device, biotechnology, and cosmetic companies. Stand up healthcare compliance programs for pharmaceutical and medical device manufacturers and related healthcare compliance policies and codes of conduct. Served as interim Chief Compliance Officer for a pharmaceutical manufacturer for a two year period and managed all aspects of the company healthcare compliance program. Conducted internal investigations into potential FDA GCP, GMP, and healthcare compliance policy violations. Led risk assessments of healthcare regulatory compliance programs and policies and advised on compliance with FDA regulations, HHS OIG Compliance Program Guidance, and the PhRMA and AdvaMed Codes on Interactions with Healthcare Professionals.","searchable_name":"Nikki Reeves","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null},{"id":426491,"version":1,"owner_type":"Person","owner_id":3883,"payload":{"bio":"\u003cp\u003eAdam Reinke represents companies in\u0026nbsp;high stakes consumer-related litigation across a broad range of industries, including automotive, healthcare, technology, and retail products.[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eAdam defends\u0026nbsp;product manufacturers and retailers in their most significant consumer-related litigation, including consumer fraud class actions, state attorney general litigation, and MDLs and other mass actions.\u0026nbsp;He has litigated all phases of both individual and class action cases, from pre-suit demands through trial and appeals, and has\u0026nbsp;served as strategic and coordinating counsel advising product manufacturers on large dockets of consumer cases in some of the country\u0026rsquo;s most challenging jurisdictions. In addition to this work,\u0026nbsp;Adam maintains a robust pro bono practice litigating for the rights of members of the LGBTQ+ community. Adam was recognized as a \"Rising Star\" by the\u0026nbsp;Minority Corporate Counsel Association\u0026nbsp;in 2024 and as one of the \"40 Best LGBTQ+ Lawyers Under 40\" by the LGBTQ+ Bar in 2023.\u003c/p\u003e\n\u003cp\u003eAdam\u0026nbsp;graduated first in his class from Emory University School of Law.\u0026nbsp;\u0026nbsp;While in law school, Adam served as the Executive Articles Editor of the\u0026nbsp;\u003cem\u003eEmory Law Journal\u003c/em\u003e.\u0026nbsp; After law school, Adam\u0026nbsp;clerked for the Honorable Edward E. Carnes, Chief Judge of the United States Court of Appeals for the Eleventh Circuit.\u003c/p\u003e","slug":"adam-reinke","email":"areinke@kslaw.com","phone":null,"matters":["\u003cp\u003eRepresenting \u003cstrong\u003eGeneral Motors\u003c/strong\u003e in various multi-state class actions alleging breach of warranty, fraud, and violations of state consumer protection laws\u003c/p\u003e","\u003cp\u003eRepresenting\u0026nbsp;\u003cstrong\u003eTikTok\u003c/strong\u003e\u0026nbsp;in the Social Media Addiction MDL against claims brought by various school districts\u003c/p\u003e","\u003cp\u003eRepresenting \u003cstrong\u003eBoehringer Ingelheim\u003c/strong\u003e in a MDL and state-court litigation arising from allegations that a drug manufactured and sold by the company causes cancer\u003c/p\u003e","\u003cp\u003eRepresenting \u003cstrong\u003ea large U.S. automobile manufacturer\u003c/strong\u003e as strategic and coordinating counsel in thousands of individual consumer fraud and breach of warranty cases\u003c/p\u003e","\u003cp\u003eManaged the defense of 2000+ individual consumer fraud and breach of warranty cases filed against \u003cstrong\u003ea large U.S. automobile manufacturer\u003c/strong\u003e, which resulted in a defense verdict in the company's first such trial in five-plus years, as well as the successful implementation of a mass settlement program\u003c/p\u003e","\u003cp\u003eRepresented \u003cstrong\u003eSmileDirectClub\u003c/strong\u003e in a lawsuit filed against the Georgia Board of Dentistry for alleged antitrust and constitutional violations\u003c/p\u003e","\u003cp\u003eRepresented \u003cstrong\u003eKimberly-Clark Corporation\u003c/strong\u003e and \u003cstrong\u003eHalyard Health\u003c/strong\u003e in litigation, including a putative class action and trial, challenging the design, labeling, and marketing of Class II medical devices\u003c/p\u003e"],"taggings":{"tags":[],"meta_tags":[]},"expertise":[{"id":74,"guid":"74.capabilities","index":0,"source":"capabilities"},{"id":764,"guid":"764.smart_tags","index":1,"source":"smartTags"},{"id":3,"guid":"3.capabilities","index":2,"source":"capabilities"},{"id":106,"guid":"106.capabilities","index":3,"source":"capabilities"},{"id":103,"guid":"103.capabilities","index":4,"source":"capabilities"},{"id":17,"guid":"17.capabilities","index":5,"source":"capabilities"}],"is_active":true,"last_name":"Reinke","nick_name":"Adam","clerkships":[{"name":"Law Clerk, Hon. 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In addition to this work,\u0026nbsp;Adam maintains a robust pro bono practice litigating for the rights of members of the LGBTQ+ community. Adam was recognized as a \"Rising Star\" by the\u0026nbsp;Minority Corporate Counsel Association\u0026nbsp;in 2024 and as one of the \"40 Best LGBTQ+ Lawyers Under 40\" by the LGBTQ+ Bar in 2023.\u003c/p\u003e\n\u003cp\u003eAdam\u0026nbsp;graduated first in his class from Emory University School of Law.\u0026nbsp;\u0026nbsp;While in law school, Adam served as the Executive Articles Editor of the\u0026nbsp;\u003cem\u003eEmory Law Journal\u003c/em\u003e.\u0026nbsp; After law school, Adam\u0026nbsp;clerked for the Honorable Edward E. Carnes, Chief Judge of the United States Court of Appeals for the Eleventh Circuit.\u003c/p\u003e","matters":["\u003cp\u003eRepresenting \u003cstrong\u003eGeneral Motors\u003c/strong\u003e in various multi-state class actions alleging breach of warranty, fraud, and violations of state consumer protection laws\u003c/p\u003e","\u003cp\u003eRepresenting\u0026nbsp;\u003cstrong\u003eTikTok\u003c/strong\u003e\u0026nbsp;in the Social Media Addiction MDL against claims brought by various school districts\u003c/p\u003e","\u003cp\u003eRepresenting \u003cstrong\u003eBoehringer Ingelheim\u003c/strong\u003e in a MDL and state-court litigation arising from allegations that a drug manufactured and sold by the company causes cancer\u003c/p\u003e","\u003cp\u003eRepresenting \u003cstrong\u003ea large U.S. automobile manufacturer\u003c/strong\u003e as strategic and coordinating counsel in thousands of individual consumer fraud and breach of warranty cases\u003c/p\u003e","\u003cp\u003eManaged the defense of 2000+ individual consumer fraud and breach of warranty cases filed against \u003cstrong\u003ea large U.S. automobile manufacturer\u003c/strong\u003e, which resulted in a defense verdict in the company's first such trial in five-plus years, as well as the successful implementation of a mass settlement program\u003c/p\u003e","\u003cp\u003eRepresented \u003cstrong\u003eSmileDirectClub\u003c/strong\u003e in a lawsuit filed against the Georgia Board of Dentistry for alleged antitrust and constitutional violations\u003c/p\u003e","\u003cp\u003eRepresented \u003cstrong\u003eKimberly-Clark Corporation\u003c/strong\u003e and \u003cstrong\u003eHalyard Health\u003c/strong\u003e in litigation, including a putative class action and trial, challenging the design, labeling, and marketing of Class II medical devices\u003c/p\u003e"],"recognitions":[{"title":"Rising Star","detail":"Minority Corporate Counsel Association, 2024"},{"title":"Recognized as a \"Next Generation Partner\" in the \"Transport: Rail and Road Litigation\" category","detail":"Legal 500 US, 2024"},{"title":"40 Best LGBTQ+ Lawyers Under 40","detail":"The LGBTQ+ Bar, 2023"},{"title":"Recognized in the \"Product Liability - Defendant\" category","detail":"Best Lawyers: Ones to Watch in America, 2023-2024"},{"title":"Recognized as a \"Next Generation Lawyer\" in the \"Transport: Rail and Road Litigation and Regulation\" category","detail":"Legal 500 US, 2023"}]},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":11827}]},"capability_group_id":3},"created_at":"2025-05-26T04:53:49.000Z","updated_at":"2025-05-26T04:53:49.000Z","searchable_text":"Reinke{{ FIELD }}{:title=\u0026gt;\"Rising Star\", :detail=\u0026gt;\"Minority Corporate Counsel Association, 2024\"}{{ FIELD }}{:title=\u0026gt;\"Recognized as a \\\"Next Generation Partner\\\" in the \\\"Transport: Rail and Road Litigation\\\" category\", :detail=\u0026gt;\"Legal 500 US, 2024\"}{{ FIELD }}{:title=\u0026gt;\"40 Best LGBTQ+ Lawyers Under 40\", :detail=\u0026gt;\"The LGBTQ+ Bar, 2023\"}{{ FIELD }}{:title=\u0026gt;\"Recognized in the \\\"Product Liability - Defendant\\\" category\", :detail=\u0026gt;\"Best Lawyers: Ones to Watch in America, 2023-2024\"}{{ FIELD }}{:title=\u0026gt;\"Recognized as a \\\"Next Generation Lawyer\\\" in the \\\"Transport: Rail and Road Litigation and Regulation\\\" category\", :detail=\u0026gt;\"Legal 500 US, 2023\"}{{ FIELD }}Representing General Motors in various multi-state class actions alleging breach of warranty, fraud, and violations of state consumer protection laws{{ FIELD }}Representing TikTok in the Social Media Addiction MDL against claims brought by various school districts{{ FIELD }}Representing Boehringer Ingelheim in a MDL and state-court litigation arising from allegations that a drug manufactured and sold by the company causes cancer{{ FIELD }}Representing a large U.S. automobile manufacturer as strategic and coordinating counsel in thousands of individual consumer fraud and breach of warranty cases{{ FIELD }}Managed the defense of 2000+ individual consumer fraud and breach of warranty cases filed against a large U.S. automobile manufacturer, which resulted in a defense verdict in the company's first such trial in five-plus years, as well as the successful implementation of a mass settlement program{{ FIELD }}Represented SmileDirectClub in a lawsuit filed against the Georgia Board of Dentistry for alleged antitrust and constitutional violations{{ FIELD }}Represented Kimberly-Clark Corporation and Halyard Health in litigation, including a putative class action and trial, challenging the design, labeling, and marketing of Class II medical devices{{ FIELD }}Adam Reinke represents companies in high stakes consumer-related litigation across a broad range of industries, including automotive, healthcare, technology, and retail products.\nAdam defends product manufacturers and retailers in their most significant consumer-related litigation, including consumer fraud class actions, state attorney general litigation, and MDLs and other mass actions. He has litigated all phases of both individual and class action cases, from pre-suit demands through trial and appeals, and has served as strategic and coordinating counsel advising product manufacturers on large dockets of consumer cases in some of the country’s most challenging jurisdictions. In addition to this work, Adam maintains a robust pro bono practice litigating for the rights of members of the LGBTQ+ community. Adam was recognized as a \"Rising Star\" by the Minority Corporate Counsel Association in 2024 and as one of the \"40 Best LGBTQ+ Lawyers Under 40\" by the LGBTQ+ Bar in 2023.\nAdam graduated first in his class from Emory University School of Law.  While in law school, Adam served as the Executive Articles Editor of the Emory Law Journal.  After law school, Adam clerked for the Honorable Edward E. Carnes, Chief Judge of the United States Court of Appeals for the Eleventh Circuit. Partner Rising Star Minority Corporate Counsel Association, 2024 Recognized as a \"Next Generation Partner\" in the \"Transport: Rail and Road Litigation\" category Legal 500 US, 2024 40 Best LGBTQ+ Lawyers Under 40 The LGBTQ+ Bar, 2023 Recognized in the \"Product Liability - Defendant\" category Best Lawyers: Ones to Watch in America, 2023-2024 Recognized as a \"Next Generation Lawyer\" in the \"Transport: Rail and Road Litigation and Regulation\" category Legal 500 US, 2023 University of Florida Levin College of Law Emory University Emory University School of Law U.S. Court of Appeals for the Eleventh Circuit U.S. District Court for the Eastern District of Michigan U.S. District Court for the Middle District of Georgia U.S. District Court for the Northern District of Georgia Georgia Court of Appeals of Georgia Supreme Court of Georgia Law Clerk, Hon. Edward E. Carnes, U.S. Court of Appeals for the Eleventh Circuit Representing General Motors in various multi-state class actions alleging breach of warranty, fraud, and violations of state consumer protection laws Representing TikTok in the Social Media Addiction MDL against claims brought by various school districts Representing Boehringer Ingelheim in a MDL and state-court litigation arising from allegations that a drug manufactured and sold by the company causes cancer Representing a large U.S. automobile manufacturer as strategic and coordinating counsel in thousands of individual consumer fraud and breach of warranty cases Managed the defense of 2000+ individual consumer fraud and breach of warranty cases filed against a large U.S. automobile manufacturer, which resulted in a defense verdict in the company's first such trial in five-plus years, as well as the successful implementation of a mass settlement program Represented SmileDirectClub in a lawsuit filed against the Georgia Board of Dentistry for alleged antitrust and constitutional violations Represented Kimberly-Clark Corporation and Halyard Health in litigation, including a putative class action and trial, challenging the design, labeling, and marketing of Class II medical devices","searchable_name":"Adam Reinke","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":35,"capability_group_featured":null,"home_page_featured":null},{"id":446168,"version":1,"owner_type":"Person","owner_id":2009,"payload":{"bio":"\u003cp\u003eTracie Renfroe has a national trial practice focusing on defense of toxic tort, environmental, product liability and other mass torts. Fortune 100 clients in the energy, manufacturing, retail, and pharmaceutical sectors around the country rely on her for trial strategy and advocacy. She\u0026nbsp;represents clients in federal and state civil jury trials, MDLs and state court coordinated actions, class actions, arbitrations, and administrative agency proceedings. She also\u0026nbsp;Chairs King \u0026amp; Spalding's Global Energy Practice and\u0026nbsp;is Managing Partner of the firm\u0026rsquo;s Houston office.[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eTracie is particularly known for presenting complex scientific and technical issues to judges, juries and arbitration panels.\u0026nbsp;She has obtained or contributed to favorable verdicts and awards for Shell Oil Company, Chevron USA, ConocoPhillips, and Johnson \u0026amp; Johnson, among others.\u003c/p\u003e\n\u003cp\u003eTracie was inducted into the American Board of Trial Advocates in 2023, and has received recognition for her advocacy and litigation skills in environmental, mass torts and product liability cases from\u0026nbsp;\u003cem\u003eChambers USA, Law 360, Legal 500, Benchmark Litigation, The Best Lawyers in America, ILO Client Choice Awards, Corporate Counsel\u0026nbsp;\u003c/em\u003eand\u0026nbsp;\u003cem\u003eSuper Lawyers.\u0026nbsp;\u003c/em\u003e\u003c/p\u003e","slug":"tracie-renfroe","email":"trenfroe@kslaw.com","phone":"+1 713 503 1261","matters":["\u003cp\u003eObtained favorable verdicts on behalf of \u003cstrong data-redactor-tag=\"strong\"\u003eShell Oil Company\u003c/strong\u003e in 2016, 2013 and 2010 in California drinking water contamination trials.\u003c/p\u003e","\u003cp\u003eLead counsel for \u003cstrong data-redactor-tag=\"strong\"\u003eConocoPhillips affiliate\u003c/strong\u003e in successful international arbitration case relating to alleged environmental contamination from oilfield operations in Ecuador.\u003c/p\u003e","\u003cp\u003eRepresenting \u003cstrong data-redactor-tag=\"strong\"\u003eDePuy,\u003c/strong\u003e a Johnson \u0026amp; Johnson company, in multi-district litigation involving metal-on-metal hip implants.\u003c/p\u003e"],"taggings":{"tags":[],"meta_tags":[]},"expertise":[{"id":102,"guid":"102.capabilities","index":0,"source":"capabilities"},{"id":107,"guid":"107.capabilities","index":1,"source":"capabilities"},{"id":103,"guid":"103.capabilities","index":2,"source":"capabilities"},{"id":761,"guid":"761.smart_tags","index":3,"source":"smartTags"},{"id":17,"guid":"17.capabilities","index":4,"source":"capabilities"},{"id":16,"guid":"16.capabilities","index":5,"source":"capabilities"},{"id":74,"guid":"74.capabilities","index":6,"source":"capabilities"},{"id":106,"guid":"106.capabilities","index":7,"source":"capabilities"},{"id":984,"guid":"984.smart_tags","index":8,"source":"smartTags"},{"id":970,"guid":"970.smart_tags","index":9,"source":"smartTags"},{"id":111,"guid":"111.capabilities","index":10,"source":"capabilities"},{"id":112,"guid":"112.capabilities","index":11,"source":"capabilities"},{"id":1143,"guid":"1143.smart_tags","index":12,"source":"smartTags"},{"id":125,"guid":"125.capabilities","index":13,"source":"capabilities"},{"id":1206,"guid":"1206.smart_tags","index":14,"source":"smartTags"},{"id":1236,"guid":"1236.smart_tags","index":15,"source":"smartTags"},{"id":1256,"guid":"1256.smart_tags","index":16,"source":"smartTags"},{"id":131,"guid":"131.capabilities","index":17,"source":"capabilities"},{"id":1248,"guid":"1248.smart_tags","index":18,"source":"smartTags"},{"id":750,"guid":"750.smart_tags","index":19,"source":"smartTags"}],"is_active":true,"last_name":"Renfroe","nick_name":"Tracie","clerkships":[],"first_name":"Tracie","title_rank":9999,"updated_by":202,"law_schools":[],"middle_name":"J.","name_suffix":"","recognitions":[{"title":"\"Tracie is a great trial lawyer with a lot of terrific experience.\" \"She is a very good environmental litigator.\"","detail":"Chambers USA, 2022"},{"title":"“Able to explain extremely complicated technical issues.\"","detail":"Chambers USA, 2019"},{"title":"“A very great trial lawyer, highly skilled at executing different strategies.”","detail":"Chambers USA, 2019"},{"title":"\"A strategic decision maker, a wonderful trial lawyer who thinks well on her feet and a great orator.”","detail":"Chambers USA, 2017"},{"title":"Named Leading Lawyer, Energy litigation: oil and gas, Environment: litigation","detail":"Legal 500, 2023"},{"title":"Named Leading Lawyer, Energy litigation: oil and gas","detail":"Legal 500, 2022"},{"title":"Named Noted Lawyer, Product liability, mass tort, and class actions: toxic tort: defense","detail":"Legal 500, 2023"},{"title":"Named to annual list of the Top 250 Women in Litigation","detail":"Benchmark Litigation, 2012-2022"},{"title":"Named a Litigation Star for Texas - Highly Recommended","detail":"Benchmark Litigation, 2019, 2024"},{"title":"Environmental Litigation Attorney","detail":"Texas Super Lawyers, 2003-2019"},{"title":"Recognized for work in Environmental Litigation","detail":"The Best Lawyers in America, 2007-2024"}],"linked_in_url":"https://www.linkedin.com/in/tracie-renfroe-59493a34/","seodescription":null,"primary_title_id":53,"translated_fields":{"en":{"bio":"\u003cp\u003eTracie Renfroe has a national trial practice focusing on defense of toxic tort, environmental, product liability and other mass torts. Fortune 100 clients in the energy, manufacturing, retail, and pharmaceutical sectors around the country rely on her for trial strategy and advocacy. She\u0026nbsp;represents clients in federal and state civil jury trials, MDLs and state court coordinated actions, class actions, arbitrations, and administrative agency proceedings. She also\u0026nbsp;Chairs King \u0026amp; Spalding's Global Energy Practice and\u0026nbsp;is Managing Partner of the firm\u0026rsquo;s Houston office.[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eTracie is particularly known for presenting complex scientific and technical issues to judges, juries and arbitration panels.\u0026nbsp;She has obtained or contributed to favorable verdicts and awards for Shell Oil Company, Chevron USA, ConocoPhillips, and Johnson \u0026amp; Johnson, among others.\u003c/p\u003e\n\u003cp\u003eTracie was inducted into the American Board of Trial Advocates in 2023, and has received recognition for her advocacy and litigation skills in environmental, mass torts and product liability cases from\u0026nbsp;\u003cem\u003eChambers USA, Law 360, Legal 500, Benchmark Litigation, The Best Lawyers in America, ILO Client Choice Awards, Corporate Counsel\u0026nbsp;\u003c/em\u003eand\u0026nbsp;\u003cem\u003eSuper Lawyers.\u0026nbsp;\u003c/em\u003e\u003c/p\u003e","matters":["\u003cp\u003eObtained favorable verdicts on behalf of \u003cstrong data-redactor-tag=\"strong\"\u003eShell Oil Company\u003c/strong\u003e in 2016, 2013 and 2010 in California drinking water contamination trials.\u003c/p\u003e","\u003cp\u003eLead counsel for \u003cstrong data-redactor-tag=\"strong\"\u003eConocoPhillips affiliate\u003c/strong\u003e in successful international arbitration case relating to alleged environmental contamination from oilfield operations in Ecuador.\u003c/p\u003e","\u003cp\u003eRepresenting \u003cstrong data-redactor-tag=\"strong\"\u003eDePuy,\u003c/strong\u003e a Johnson \u0026amp; Johnson company, in multi-district litigation involving metal-on-metal hip implants.\u003c/p\u003e"],"recognitions":[{"title":"\"Tracie is a great trial lawyer with a lot of terrific experience.\" \"She is a very good environmental litigator.\"","detail":"Chambers USA, 2022"},{"title":"“Able to explain extremely complicated technical issues.\"","detail":"Chambers USA, 2019"},{"title":"“A very great trial lawyer, highly skilled at executing different strategies.”","detail":"Chambers USA, 2019"},{"title":"\"A strategic decision maker, a wonderful trial lawyer who thinks well on her feet and a great orator.”","detail":"Chambers USA, 2017"},{"title":"Named Leading Lawyer, Energy litigation: oil and gas, Environment: litigation","detail":"Legal 500, 2023"},{"title":"Named Leading Lawyer, Energy litigation: oil and gas","detail":"Legal 500, 2022"},{"title":"Named Noted Lawyer, Product liability, mass tort, and class actions: toxic tort: defense","detail":"Legal 500, 2023"},{"title":"Named to annual list of the Top 250 Women in Litigation","detail":"Benchmark Litigation, 2012-2022"},{"title":"Named a Litigation Star for Texas - Highly Recommended","detail":"Benchmark Litigation, 2019, 2024"},{"title":"Environmental Litigation Attorney","detail":"Texas Super Lawyers, 2003-2019"},{"title":"Recognized for work in Environmental Litigation","detail":"The Best Lawyers in America, 2007-2024"}]},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":5214}]},"capability_group_id":3},"created_at":"2026-02-25T20:27:35.000Z","updated_at":"2026-02-25T20:27:35.000Z","searchable_text":"Renfroe{{ FIELD }}{:title=\u0026gt;\"\\\"Tracie is a great trial lawyer with a lot of terrific experience.\\\" \\\"She is a very good environmental litigator.\\\"\", :detail=\u0026gt;\"Chambers USA, 2022\"}{{ FIELD }}{:title=\u0026gt;\"“Able to explain extremely complicated technical issues.\\\"\", :detail=\u0026gt;\"Chambers USA, 2019\"}{{ FIELD }}{:title=\u0026gt;\"“A very great trial lawyer, highly skilled at executing different strategies.”\", :detail=\u0026gt;\"Chambers USA, 2019\"}{{ FIELD }}{:title=\u0026gt;\"\\\"A strategic decision maker, a wonderful trial lawyer who thinks well on her feet and a great orator.”\", :detail=\u0026gt;\"Chambers USA, 2017\"}{{ FIELD }}{:title=\u0026gt;\"Named Leading Lawyer, Energy litigation: oil and gas, Environment: litigation\", :detail=\u0026gt;\"Legal 500, 2023\"}{{ FIELD }}{:title=\u0026gt;\"Named Leading Lawyer, Energy litigation: oil and gas\", :detail=\u0026gt;\"Legal 500, 2022\"}{{ FIELD }}{:title=\u0026gt;\"Named Noted Lawyer, Product liability, mass tort, and class actions: toxic tort: defense\", :detail=\u0026gt;\"Legal 500, 2023\"}{{ FIELD }}{:title=\u0026gt;\"Named to annual list of the Top 250 Women in Litigation\", :detail=\u0026gt;\"Benchmark Litigation, 2012-2022\"}{{ FIELD }}{:title=\u0026gt;\"Named a Litigation Star for Texas - Highly Recommended\", :detail=\u0026gt;\"Benchmark Litigation, 2019, 2024\"}{{ FIELD }}{:title=\u0026gt;\"Environmental Litigation Attorney\", :detail=\u0026gt;\"Texas Super Lawyers, 2003-2019\"}{{ FIELD }}{:title=\u0026gt;\"Recognized for work in Environmental Litigation\", :detail=\u0026gt;\"The Best Lawyers in America, 2007-2024\"}{{ FIELD }}Obtained favorable verdicts on behalf of Shell Oil Company in 2016, 2013 and 2010 in California drinking water contamination trials.{{ FIELD }}Lead counsel for ConocoPhillips affiliate in successful international arbitration case relating to alleged environmental contamination from oilfield operations in Ecuador.{{ FIELD }}Representing DePuy, a Johnson \u0026amp; Johnson company, in multi-district litigation involving metal-on-metal hip implants.{{ FIELD }}Tracie Renfroe has a national trial practice focusing on defense of toxic tort, environmental, product liability and other mass torts. Fortune 100 clients in the energy, manufacturing, retail, and pharmaceutical sectors around the country rely on her for trial strategy and advocacy. She represents clients in federal and state civil jury trials, MDLs and state court coordinated actions, class actions, arbitrations, and administrative agency proceedings. She also Chairs King \u0026amp; Spalding's Global Energy Practice and is Managing Partner of the firm’s Houston office.\nTracie is particularly known for presenting complex scientific and technical issues to judges, juries and arbitration panels. She has obtained or contributed to favorable verdicts and awards for Shell Oil Company, Chevron USA, ConocoPhillips, and Johnson \u0026amp; Johnson, among others.\nTracie was inducted into the American Board of Trial Advocates in 2023, and has received recognition for her advocacy and litigation skills in environmental, mass torts and product liability cases from Chambers USA, Law 360, Legal 500, Benchmark Litigation, The Best Lawyers in America, ILO Client Choice Awards, Corporate Counsel and Super Lawyers.  Partner \"Tracie is a great trial lawyer with a lot of terrific experience.\" \"She is a very good environmental litigator.\" Chambers USA, 2022 “Able to explain extremely complicated technical issues.\" Chambers USA, 2019 “A very great trial lawyer, highly skilled at executing different strategies.” Chambers USA, 2019 \"A strategic decision maker, a wonderful trial lawyer who thinks well on her feet and a great orator.” Chambers USA, 2017 Named Leading Lawyer, Energy litigation: oil and gas, Environment: litigation Legal 500, 2023 Named Leading Lawyer, Energy litigation: oil and gas Legal 500, 2022 Named Noted Lawyer, Product liability, mass tort, and class actions: toxic tort: defense Legal 500, 2023 Named to annual list of the Top 250 Women in Litigation Benchmark Litigation, 2012-2022 Named a Litigation Star for Texas - Highly Recommended Benchmark Litigation, 2019, 2024 Environmental Litigation Attorney Texas Super Lawyers, 2003-2019 Recognized for work in Environmental Litigation The Best Lawyers in America, 2007-2024 Baylor University Baylor University School of Law Baylor University Baylor University School of Law Supreme Court of the United States U.S. Court of Appeals for the First Circuit U.S. Court of Appeals for the Fifth Circuit U.S. Court of Appeals for the Ninth Circuit U.S. District Court for the Eastern District of Texas U.S. District Court for the Northern District of Texas U.S. District Court for the Southern District of Texas U.S. District Court for the Western District of Texas Texas American Board of Trial Advocates American College of Environmental Lawyers State Bar of Texas: Litigation Section, Natural Resources \u0026amp; Env. Section; American Bar Association: Litigation Section, Natural Resources \u0026amp; Env. Section; Bar Association of the Fifth Federal Circuit; Texas Bar Foundation, Continuing Life Fellow; IADC Diversity Law Institute Trial Law Institute Institute for Energy Law of the Center for American and International Law, Executive Committee United Way of Greater Houston, Board of Trustees 2020-2023 Obtained favorable verdicts on behalf of Shell Oil Company in 2016, 2013 and 2010 in California drinking water contamination trials. Lead counsel for ConocoPhillips affiliate in successful international arbitration case relating to alleged environmental contamination from oilfield operations in Ecuador. Representing DePuy, a Johnson \u0026amp; Johnson company, in multi-district litigation involving metal-on-metal hip implants.","searchable_name":"Tracie J. Renfroe","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null},{"id":446872,"version":1,"owner_type":"Person","owner_id":3988,"payload":{"bio":"\u003cp\u003eGregory Ruehlmann is a partner in the Atlanta office and a member of the firm\u0026rsquo;s Trial practice, where he focuses on high-profile product-liability, class-action,\u0026nbsp;and other mass-tort litigation.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eGregory has developed considerable experience in nationwide defense of clients in the life-science, technology, automotive, and consumer-product sectors at all stages of litigation\u0026mdash;from initial assessment and case strategy to offensive and defensive discovery and deposition-taking up to and including working on multiple core trial teams. Gregory has argued several successful dispositive motions and \u003cem\u003eDaubert\u003c/em\u003e challenges in courts throughout the nation, but is equally focused on developing the themes, facts, and testimony necessary for victory at trial.\u003c/p\u003e\n\u003cp\u003eIn addition to tort and product-liability work, Gregory has experience in litigating a wide range of business and intellectual-property disputes and conducting risk assessments and other internal investigations. A fluent German speaker, he counsels clients based in German-speaking countries on navigating the U.S. litigation and regulatory systems.\u003c/p\u003e\n\u003cp\u003eGregory\u0026nbsp;maintains a robust\u0026nbsp;\u003cem\u003epro bono \u003c/em\u003epractice. He has successfully represented asylum seekers through the Georgia Asylum and Immigration Network (GAIN) and defends small business owners through Atlanta's Rice Innovation Center for Entrepreneurs (RICE).\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003ePublications\u003c/strong\u003e\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eManaging editor, \u003cem\u003eThe Regulation of Pharmaceutical Manufacturers \u003c/em\u003e(3d ed.), Fastcase\u003c/li\u003e\n\u003cli\u003eLead author of \u0026ldquo;The Trial of a Drug or Device Case,\u0026rdquo; in \u003cem\u003eDrug \u0026amp; Device Product Liability Litigation Strategy \u003c/em\u003e(3d ed. 2026), Oxford Univ. Press\u003c/li\u003e\n\u003c/ul\u003e","slug":"gregory-ruehlmann","email":"gruehlmann@kslaw.com","phone":null,"matters":["\u003cp\u003eDefending\u0026nbsp;\u003cstrong\u003eBoehringer Ingelheim\u0026nbsp;\u003c/strong\u003ein multiple class actions arising from allegations concerning Zantac and other ranitidine-containing products\u003c/p\u003e","\u003cp\u003e\u003cstrong\u003e\u003cem\u003eLife Sciences\u003c/em\u003e\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eDefending\u0026nbsp;\u003cstrong\u003eColoplast\u003c/strong\u003e\u0026nbsp;in nationwide product-liability litigation relating to injuries allegedly caused by the company\u0026rsquo;s female pelvic-mesh devices.\u003c/p\u003e","\u003cp\u003eDefending\u0026nbsp;\u003cstrong\u003eKimberly-Clark\u003c/strong\u003e\u0026nbsp;and\u0026nbsp;\u003cstrong\u003eHalyard Health\u003c/strong\u003e\u0026nbsp;in a class action concerning the design, labeling, and advertising of a Class II medical device.\u003c/p\u003e","\u003cp\u003eDefended\u0026nbsp;\u003cstrong\u003eGlaxoSmithKline\u003c/strong\u003e\u0026nbsp;in nationwide litigation concerning allegations of injuries from use of the company\u0026rsquo;s antidepressant medication.\u003c/p\u003e","\u003cp\u003e\u003cstrong\u003e\u003cem\u003eAutomotive\u003c/em\u003e\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eDefended\u0026nbsp;\u003cstrong\u003ea leading automobile manufacturer\u003c/strong\u003e\u0026nbsp;in hundreds of consumer-fraud cases in California.\u003c/p\u003e","\u003cp\u003e\u003cstrong\u003e\u003cem\u003eConsumer Products\u003c/em\u003e\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eDefended\u0026nbsp;\u003cstrong\u003ea leading international consumer-product manufacturer\u003c/strong\u003e\u0026nbsp;in multiple actions relating to alleged injuries from the company\u0026rsquo;s laundry detergent pods.\u003c/p\u003e"],"taggings":{"tags":[],"meta_tags":[]},"expertise":[{"id":74,"guid":"74.capabilities","index":0,"source":"capabilities"},{"id":103,"guid":"103.capabilities","index":1,"source":"capabilities"},{"id":17,"guid":"17.capabilities","index":2,"source":"capabilities"},{"id":16,"guid":"16.capabilities","index":3,"source":"capabilities"},{"id":3,"guid":"3.capabilities","index":4,"source":"capabilities"},{"id":1303,"guid":"1303.smart_tags","index":5,"source":"smartTags"},{"id":970,"guid":"970.smart_tags","index":6,"source":"smartTags"}],"is_active":true,"last_name":"Ruehlmann","nick_name":"Gregory","clerkships":[],"first_name":"Gregory","title_rank":9999,"updated_by":202,"law_schools":[{"id":1451,"meta":{"degree":"J.D.","honors":"cum laude","is_law_school":"1","graduation_date":"2012-01-01 00:00:00"},"order":1,"pin_order":null,"pin_expiration":null}],"middle_name":"A.","name_suffix":"","recognitions":null,"linked_in_url":"https://www.linkedin.com/in/gregory-ruehlmann-866a576/","seodescription":null,"primary_title_id":15,"translated_fields":{"en":{"bio":"\u003cp\u003eGregory Ruehlmann is a partner in the Atlanta office and a member of the firm\u0026rsquo;s Trial practice, where he focuses on high-profile product-liability, class-action,\u0026nbsp;and other mass-tort litigation.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eGregory has developed considerable experience in nationwide defense of clients in the life-science, technology, automotive, and consumer-product sectors at all stages of litigation\u0026mdash;from initial assessment and case strategy to offensive and defensive discovery and deposition-taking up to and including working on multiple core trial teams. Gregory has argued several successful dispositive motions and \u003cem\u003eDaubert\u003c/em\u003e challenges in courts throughout the nation, but is equally focused on developing the themes, facts, and testimony necessary for victory at trial.\u003c/p\u003e\n\u003cp\u003eIn addition to tort and product-liability work, Gregory has experience in litigating a wide range of business and intellectual-property disputes and conducting risk assessments and other internal investigations. A fluent German speaker, he counsels clients based in German-speaking countries on navigating the U.S. litigation and regulatory systems.\u003c/p\u003e\n\u003cp\u003eGregory\u0026nbsp;maintains a robust\u0026nbsp;\u003cem\u003epro bono \u003c/em\u003epractice. He has successfully represented asylum seekers through the Georgia Asylum and Immigration Network (GAIN) and defends small business owners through Atlanta's Rice Innovation Center for Entrepreneurs (RICE).\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003ePublications\u003c/strong\u003e\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eManaging editor, \u003cem\u003eThe Regulation of Pharmaceutical Manufacturers \u003c/em\u003e(3d ed.), Fastcase\u003c/li\u003e\n\u003cli\u003eLead author of \u0026ldquo;The Trial of a Drug or Device Case,\u0026rdquo; in \u003cem\u003eDrug \u0026amp; Device Product Liability Litigation Strategy \u003c/em\u003e(3d ed. 2026), Oxford Univ. Press\u003c/li\u003e\n\u003c/ul\u003e","matters":["\u003cp\u003eDefending\u0026nbsp;\u003cstrong\u003eBoehringer Ingelheim\u0026nbsp;\u003c/strong\u003ein multiple class actions arising from allegations concerning Zantac and other ranitidine-containing products\u003c/p\u003e","\u003cp\u003e\u003cstrong\u003e\u003cem\u003eLife Sciences\u003c/em\u003e\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eDefending\u0026nbsp;\u003cstrong\u003eColoplast\u003c/strong\u003e\u0026nbsp;in nationwide product-liability litigation relating to injuries allegedly caused by the company\u0026rsquo;s female pelvic-mesh devices.\u003c/p\u003e","\u003cp\u003eDefending\u0026nbsp;\u003cstrong\u003eKimberly-Clark\u003c/strong\u003e\u0026nbsp;and\u0026nbsp;\u003cstrong\u003eHalyard Health\u003c/strong\u003e\u0026nbsp;in a class action concerning the design, labeling, and advertising of a Class II medical device.\u003c/p\u003e","\u003cp\u003eDefended\u0026nbsp;\u003cstrong\u003eGlaxoSmithKline\u003c/strong\u003e\u0026nbsp;in nationwide litigation concerning allegations of injuries from use of the company\u0026rsquo;s antidepressant medication.\u003c/p\u003e","\u003cp\u003e\u003cstrong\u003e\u003cem\u003eAutomotive\u003c/em\u003e\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eDefended\u0026nbsp;\u003cstrong\u003ea leading automobile manufacturer\u003c/strong\u003e\u0026nbsp;in hundreds of consumer-fraud cases in California.\u003c/p\u003e","\u003cp\u003e\u003cstrong\u003e\u003cem\u003eConsumer Products\u003c/em\u003e\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eDefended\u0026nbsp;\u003cstrong\u003ea leading international consumer-product manufacturer\u003c/strong\u003e\u0026nbsp;in multiple actions relating to alleged injuries from the company\u0026rsquo;s laundry detergent pods.\u003c/p\u003e"]},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":4537}]},"capability_group_id":3},"created_at":"2026-03-19T20:19:09.000Z","updated_at":"2026-03-19T20:19:09.000Z","searchable_text":"Ruehlmann{{ FIELD }}Defending Boehringer Ingelheim in multiple class actions arising from allegations concerning Zantac and other ranitidine-containing products{{ FIELD }}Life Sciences\nDefending Coloplast in nationwide product-liability litigation relating to injuries allegedly caused by the company’s female pelvic-mesh devices.{{ FIELD }}Defending Kimberly-Clark and Halyard Health in a class action concerning the design, labeling, and advertising of a Class II medical device.{{ FIELD }}Defended GlaxoSmithKline in nationwide litigation concerning allegations of injuries from use of the company’s antidepressant medication.{{ FIELD }}Automotive\nDefended a leading automobile manufacturer in hundreds of consumer-fraud cases in California.{{ FIELD }}Consumer Products\nDefended a leading international consumer-product manufacturer in multiple actions relating to alleged injuries from the company’s laundry detergent pods.{{ FIELD }}Gregory Ruehlmann is a partner in the Atlanta office and a member of the firm’s Trial practice, where he focuses on high-profile product-liability, class-action, and other mass-tort litigation. \nGregory has developed considerable experience in nationwide defense of clients in the life-science, technology, automotive, and consumer-product sectors at all stages of litigation—from initial assessment and case strategy to offensive and defensive discovery and deposition-taking up to and including working on multiple core trial teams. Gregory has argued several successful dispositive motions and Daubert challenges in courts throughout the nation, but is equally focused on developing the themes, facts, and testimony necessary for victory at trial.\nIn addition to tort and product-liability work, Gregory has experience in litigating a wide range of business and intellectual-property disputes and conducting risk assessments and other internal investigations. A fluent German speaker, he counsels clients based in German-speaking countries on navigating the U.S. litigation and regulatory systems.\nGregory maintains a robust pro bono practice. He has successfully represented asylum seekers through the Georgia Asylum and Immigration Network (GAIN) and defends small business owners through Atlanta's Rice Innovation Center for Entrepreneurs (RICE).\nPublications\n\nManaging editor, The Regulation of Pharmaceutical Manufacturers (3d ed.), Fastcase\nLead author of “The Trial of a Drug or Device Case,” in Drug \u0026amp; Device Product Liability Litigation Strategy (3d ed. 2026), Oxford Univ. Press\n Partner University of Notre Dame Notre Dame Law School Northwestern University Northwestern Pritzker School of Law University of Chicago University of Chicago Law School U.S. District Court for the Northern District of Ohio U.S. District Court for the Southern District of Ohio U.S. District Court for the Northern District of Illinois U.S. District Court for the Northern District of Georgia Georgia Illinois Ohio St. Thomas More Society of Atlanta (Board) Defending Boehringer Ingelheim in multiple class actions arising from allegations concerning Zantac and other ranitidine-containing products Life Sciences\nDefending Coloplast in nationwide product-liability litigation relating to injuries allegedly caused by the company’s female pelvic-mesh devices. Defending Kimberly-Clark and Halyard Health in a class action concerning the design, labeling, and advertising of a Class II medical device. Defended GlaxoSmithKline in nationwide litigation concerning allegations of injuries from use of the company’s antidepressant medication. Automotive\nDefended a leading automobile manufacturer in hundreds of consumer-fraud cases in California. Consumer Products\nDefended a leading international consumer-product manufacturer in multiple actions relating to alleged injuries from the company’s laundry detergent pods.","searchable_name":"Gregory A. Ruehlmann","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null},{"id":441704,"version":1,"owner_type":"Person","owner_id":5505,"payload":{"bio":"\u003cp\u003eRachel Rubens is an associate in King \u0026amp; Spalding's Environmental and\u0026nbsp;Toxic Tort group\u0026nbsp;and is located in the San Francisco office. Rachel has represented corporate defendants in a wide array of complex matters in the\u0026nbsp;pharmaceutical, automotive, and chemical industries. Her practice is primarily focused on complex product liability and toxic tort litigation.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eRachel received her J.D. from University of California, Davis, where she served as an Articles Editor on the UC Davis Law Review and a competitor in the Seigenthaler-Sutherland National First Amendment Moot Court Competition.\u0026nbsp; In 2019, Rachel was an extern for the Honorable Justice Mariano Florentino Cuellar of the California Supreme Court.\u003c/p\u003e","slug":"rachel-rubens","email":"rrubens@kslaw.com","phone":null,"matters":null,"taggings":{"tags":[],"meta_tags":[]},"expertise":[{"id":74,"guid":"74.capabilities","index":0,"source":"capabilities"},{"id":17,"guid":"17.capabilities","index":1,"source":"capabilities"},{"id":16,"guid":"16.capabilities","index":2,"source":"capabilities"}],"is_active":true,"last_name":"Rubens","nick_name":"Rachel","clerkships":[],"first_name":"Rachel","title_rank":9999,"updated_by":202,"law_schools":[{"id":2160,"meta":{"degree":"J.D.","honors":"","is_law_school":"1","graduation_date":"2020-01-01 00:00:00"},"order":2,"pin_order":null,"pin_expiration":null}],"middle_name":" ","name_suffix":"","recognitions":null,"linked_in_url":"https://www.linkedin.com/in/rachel-rubens-811a56b5/","seodescription":null,"primary_title_id":2,"translated_fields":{"en":{"bio":"\u003cp\u003eRachel Rubens is an associate in King \u0026amp; Spalding's Environmental and\u0026nbsp;Toxic Tort group\u0026nbsp;and is located in the San Francisco office. Rachel has represented corporate defendants in a wide array of complex matters in the\u0026nbsp;pharmaceutical, automotive, and chemical industries. Her practice is primarily focused on complex product liability and toxic tort litigation.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eRachel received her J.D. from University of California, Davis, where she served as an Articles Editor on the UC Davis Law Review and a competitor in the Seigenthaler-Sutherland National First Amendment Moot Court Competition.\u0026nbsp; In 2019, Rachel was an extern for the Honorable Justice Mariano Florentino Cuellar of the California Supreme Court.\u003c/p\u003e"},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":9458}]},"capability_group_id":3},"created_at":"2025-10-27T19:11:24.000Z","updated_at":"2025-10-27T19:11:24.000Z","searchable_text":"Rubens{{ FIELD }}Rachel Rubens is an associate in King \u0026amp; Spalding's Environmental and Toxic Tort group and is located in the San Francisco office. Rachel has represented corporate defendants in a wide array of complex matters in the pharmaceutical, automotive, and chemical industries. Her practice is primarily focused on complex product liability and toxic tort litigation. \nRachel received her J.D. from University of California, Davis, where she served as an Articles Editor on the UC Davis Law Review and a competitor in the Seigenthaler-Sutherland National First Amendment Moot Court Competition.  In 2019, Rachel was an extern for the Honorable Justice Mariano Florentino Cuellar of the California Supreme Court. Associate University of Miami University of Miami School of Law University of Miami University of Miami School of Law University of California-Davis UC Davis School of Law U.S. District Court for the Central District of California U.S. District Court for the Northern District of California California","searchable_name":"Rachel Rubens","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null},{"id":427033,"version":1,"owner_type":"Person","owner_id":6185,"payload":{"bio":"\u003cp\u003e\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eDavid Rhee is a Senior Attorney in the Product Liability \u0026amp; Mass Torts\u0026nbsp;Practice Group.\u0026nbsp;David\u0026nbsp;focuses on providing cost effective legal\u0026nbsp;solutions and advising clients through all phases of eDiscovery.\u0026nbsp;He\u0026nbsp;delivers\u0026nbsp;efficient mechanisms for\u0026nbsp;early case assessment, document review management, and pre-production processes.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eFor over 15\u0026nbsp;years, he\u0026nbsp;has provided\u0026nbsp;ESI response strategies for government investigations, arbitration, qui tam, antitrust, class actions, pharmaceutical, biotech, and patent prosecution claims.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eDavid has acquired extensive experience utilizing several eDiscovery platforms including Concordance, DISCO, Viewpoint, and others. He is also a Relativity Certified Administrator (RCA) and Brainspace Analyst.\u003c/p\u003e\n\u003cp\u003eHe has acted as a liaison between eDiscovery vendors and clients by ensuring effective communication based on\u0026nbsp;technology and legal vernacular.\u0026nbsp;David also maintains an active pro bono practice and has provided legal representation\u0026nbsp;through several Chicago agencies including Cabrini Green Legal Aid, Domestic Violence Legal Clinic (DVLC), Center on Halsted Legal Clinic, and Lawyers for Good Government.\u003c/p\u003e","slug":"david-rhee","email":"drhee@kslaw.com","phone":null,"matters":["\u003cp\u003eProviding early case assessment strategies, database management, and review supervision in connection with several government investigations and litigation matters.\u003c/p\u003e","\u003cp\u003eParticipating in custodial interviews to determine relevant sources of electronically stored information (ESI) in response to a DOJ Request for Production.\u003c/p\u003e","\u003cp\u003ePreparing documents for rolling productions by ensuring the fulfillment of technical requirements relating to an anti-trust matter.\u003c/p\u003e","\u003cp\u003eDrafting document review protocols, preparing suitable coding layouts, and overseeing large scale review teams related to multiple whistleblower/qui tam matters.\u003c/p\u003e","\u003cp\u003eDrafting privilege log descriptions and addressing subsequent deficiencies raised by opposing counsel for a patent prosecution matter.\u003c/p\u003e","\u003cp\u003eDeveloping efficient data culling strategies and providing complex metrics in response to a Select Committee Investigation.\u003c/p\u003e"],"taggings":{"tags":[],"meta_tags":[{"id":3202}]},"expertise":[{"id":74,"guid":"74.capabilities","index":0,"source":"capabilities"},{"id":17,"guid":"17.capabilities","index":1,"source":"capabilities"}],"is_active":true,"last_name":"Rhee","nick_name":"David","clerkships":[],"first_name":"David","title_rank":9999,"updated_by":202,"law_schools":[{"id":770,"meta":{"degree":"J.D.","honors":null,"is_law_school":1,"graduation_date":null},"order":1,"pin_order":null,"pin_expiration":null}],"middle_name":"Y.","name_suffix":"","recognitions":null,"linked_in_url":null,"seodescription":"David Rhee is a Senior Attorney in the Product Liability \u0026 Mass Torts Practice Group. Read more about it.","primary_title_id":76,"translated_fields":{"en":{"bio":"\u003cp\u003e\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eDavid Rhee is a Senior Attorney in the Product Liability \u0026amp; Mass Torts\u0026nbsp;Practice Group.\u0026nbsp;David\u0026nbsp;focuses on providing cost effective legal\u0026nbsp;solutions and advising clients through all phases of eDiscovery.\u0026nbsp;He\u0026nbsp;delivers\u0026nbsp;efficient mechanisms for\u0026nbsp;early case assessment, document review management, and pre-production processes.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eFor over 15\u0026nbsp;years, he\u0026nbsp;has provided\u0026nbsp;ESI response strategies for government investigations, arbitration, qui tam, antitrust, class actions, pharmaceutical, biotech, and patent prosecution claims.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eDavid has acquired extensive experience utilizing several eDiscovery platforms including Concordance, DISCO, Viewpoint, and others. He is also a Relativity Certified Administrator (RCA) and Brainspace Analyst.\u003c/p\u003e\n\u003cp\u003eHe has acted as a liaison between eDiscovery vendors and clients by ensuring effective communication based on\u0026nbsp;technology and legal vernacular.\u0026nbsp;David also maintains an active pro bono practice and has provided legal representation\u0026nbsp;through several Chicago agencies including Cabrini Green Legal Aid, Domestic Violence Legal Clinic (DVLC), Center on Halsted Legal Clinic, and Lawyers for Good Government.\u003c/p\u003e","matters":["\u003cp\u003eProviding early case assessment strategies, database management, and review supervision in connection with several government investigations and litigation matters.\u003c/p\u003e","\u003cp\u003eParticipating in custodial interviews to determine relevant sources of electronically stored information (ESI) in response to a DOJ Request for Production.\u003c/p\u003e","\u003cp\u003ePreparing documents for rolling productions by ensuring the fulfillment of technical requirements relating to an anti-trust matter.\u003c/p\u003e","\u003cp\u003eDrafting document review protocols, preparing suitable coding layouts, and overseeing large scale review teams related to multiple whistleblower/qui tam matters.\u003c/p\u003e","\u003cp\u003eDrafting privilege log descriptions and addressing subsequent deficiencies raised by opposing counsel for a patent prosecution matter.\u003c/p\u003e","\u003cp\u003eDeveloping efficient data culling strategies and providing complex metrics in response to a Select Committee Investigation.\u003c/p\u003e"]},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":9549}]},"capability_group_id":3},"created_at":"2025-05-26T04:58:24.000Z","updated_at":"2025-05-26T04:58:24.000Z","searchable_text":"Rhee{{ FIELD }}Providing early case assessment strategies, database management, and review supervision in connection with several government investigations and litigation matters.{{ FIELD }}Participating in custodial interviews to determine relevant sources of electronically stored information (ESI) in response to a DOJ Request for Production.{{ FIELD }}Preparing documents for rolling productions by ensuring the fulfillment of technical requirements relating to an anti-trust matter.{{ FIELD }}Drafting document review protocols, preparing suitable coding layouts, and overseeing large scale review teams related to multiple whistleblower/qui tam matters.{{ FIELD }}Drafting privilege log descriptions and addressing subsequent deficiencies raised by opposing counsel for a patent prosecution matter.{{ FIELD }}Developing efficient data culling strategies and providing complex metrics in response to a Select Committee Investigation.{{ FIELD }} \nDavid Rhee is a Senior Attorney in the Product Liability \u0026amp; Mass Torts Practice Group. David focuses on providing cost effective legal solutions and advising clients through all phases of eDiscovery. He delivers efficient mechanisms for early case assessment, document review management, and pre-production processes. \nFor over 15 years, he has provided ESI response strategies for government investigations, arbitration, qui tam, antitrust, class actions, pharmaceutical, biotech, and patent prosecution claims. \nDavid has acquired extensive experience utilizing several eDiscovery platforms including Concordance, DISCO, Viewpoint, and others. He is also a Relativity Certified Administrator (RCA) and Brainspace Analyst.\nHe has acted as a liaison between eDiscovery vendors and clients by ensuring effective communication based on technology and legal vernacular. David also maintains an active pro bono practice and has provided legal representation through several Chicago agencies including Cabrini Green Legal Aid, Domestic Violence Legal Clinic (DVLC), Center on Halsted Legal Clinic, and Lawyers for Good Government. David Rhee lawyer Senior Attorney University of Michigan-Ann Arbor  Golden Gate University-San Francisco Golden Gate University School of Law U.S. District Court for the Northern District of Illinois Illinois Wisconsin Providing early case assessment strategies, database management, and review supervision in connection with several government investigations and litigation matters. Participating in custodial interviews to determine relevant sources of electronically stored information (ESI) in response to a DOJ Request for Production. Preparing documents for rolling productions by ensuring the fulfillment of technical requirements relating to an anti-trust matter. Drafting document review protocols, preparing suitable coding layouts, and overseeing large scale review teams related to multiple whistleblower/qui tam matters. Drafting privilege log descriptions and addressing subsequent deficiencies raised by opposing counsel for a patent prosecution matter. Developing efficient data culling strategies and providing complex metrics in response to a Select Committee Investigation.","searchable_name":"David Y. Rhee","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null}]}}