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He also develops business and marketing strategies that respond to ever-changing federal regulatory schemes.\u003c/p\u003e\n\u003cp\u003eA frequent author and speaker on healthcare compliance and investigations, Seth works to help clients to identify and predict burgeoning areas of enforcement. Seth has been recognized since 2008 as a top Washington, D.C. healthcare lawyer by \u003cem\u003eChambers USA\u003c/em\u003e. He has also received recognition as a leading healthcare lawyer from \u003cem\u003eExpert Guides, Guide to the Leading Healthcare Lawyers,\u003c/em\u003e Super Lawyers Washington, D.C.\u003cem\u003e,\u003c/em\u003e \u003cem\u003eBest Lawyers\u003c/em\u003e, and \u003cem\u003eWashingtonian Magazine\u003c/em\u003e's Top Lawyers rankings.\u003c/p\u003e","recognitions":[{"title":"Top Healthcare Lawyer: Washington, D.C. ","detail":"Chambers USA"},{"title":"Leading Healthcare Lawyer","detail":"Expert Guides and Guide to the Leading Healthcare Lawyers"},{"title":"Super Lawyers: Washington, D.C.","detail":""},{"title":"The Best Lawyers in America","detail":""},{"title":"Top Lawyers ","detail":"Washingtonian Magazine"},{"title":"Named to Best Lawyers in America for FDA Law","detail":"Best Lawyers in America, 2020"}]},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":1020}]},"capability_group_id":2},"created_at":"2025-05-26T04:50:49.000Z","updated_at":"2025-05-26T04:50:49.000Z","searchable_text":"Lundy{{ FIELD }}{:title=\u0026gt;\"Top Healthcare Lawyer: Washington, D.C. \", :detail=\u0026gt;\"Chambers USA\"}{{ FIELD }}{:title=\u0026gt;\"Leading Healthcare Lawyer\", :detail=\u0026gt;\"Expert Guides and Guide to the Leading Healthcare Lawyers\"}{{ FIELD }}{:title=\u0026gt;\"Super Lawyers: Washington, D.C.\", :detail=\u0026gt;\"\"}{{ FIELD }}{:title=\u0026gt;\"The Best Lawyers in America\", :detail=\u0026gt;\"\"}{{ FIELD }}{:title=\u0026gt;\"Top Lawyers \", :detail=\u0026gt;\"Washingtonian Magazine\"}{{ FIELD }}{:title=\u0026gt;\"Named to Best Lawyers in America for FDA Law\", :detail=\u0026gt;\"Best Lawyers in America, 2020\"}{{ FIELD }}Seth Lundy represents prominent medical device and pharmaceutical companies and healthcare providers, suppliers and distributors in complex legal and regulatory matters and investigations. As Deputy Chair of our FDA and Life Sciences practice, Seth is widely recognized as a leading national authority on compliance with federal and state fraud and abuse laws. His practical, business-oriented approach earns accolades as one of the industry's leading lawyers from sources including Chambers USA, LMG Life Sciences, Legal 500, Best Lawyers, and Super Lawyers.\nSeth's in-depth understanding of the industry allows him to work seamlessly with boards of directors, C-suite management, legal departments, compliance offices and operational divisions. He designs compliance programs; helps client to ensure that operations meet changing standards; defends clients in government investigations; performs internal audits; conducts corporate due diligence; and engages in civil, criminal and administrative litigation.\nSeth is experienced in working with federal regulators and legislators to create, revise and interpret healthcare-related laws, regulations and policies. He also develops business and marketing strategies that respond to ever-changing federal regulatory schemes.\nA frequent author and speaker on healthcare compliance and investigations, Seth works to help clients to identify and predict burgeoning areas of enforcement. Seth has been recognized since 2008 as a top Washington, D.C. healthcare lawyer by Chambers USA. He has also received recognition as a leading healthcare lawyer from Expert Guides, Guide to the Leading Healthcare Lawyers, Super Lawyers Washington, D.C., Best Lawyers, and Washingtonian Magazine's Top Lawyers rankings. Partner Top Healthcare Lawyer: Washington, D.C.  Chambers USA Leading Healthcare Lawyer Expert Guides and Guide to the Leading Healthcare Lawyers Super Lawyers: Washington, D.C.  The Best Lawyers in America  Top Lawyers  Washingtonian Magazine Named to Best Lawyers in America for FDA Law Best Lawyers in America, 2020 Amherst College  George Washington University George Washington University Law School District of Columbia Maryland","searchable_name":"Seth H. Lundy","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":174,"capability_group_featured":null,"home_page_featured":null},{"id":445135,"version":1,"owner_type":"Person","owner_id":6878,"payload":{"bio":"\u003cp\u003eBritt Latour is a Senior Staff Attorney in the Products Liability and Mass Torts Practice Group. Britt comes to the firm with a background in healthcare compliance and government investigations. She works closely with in-house counsel, outside counsel and vendors to develop and execute project plans for each stage of the Electronic Discovery Reference Model (EDRM) including identification, preservation, collection, review, and production of documents in complex litigation or government investigations. She collaborates with technology providers to leverage advanced tools to offer cost-effective and timely solutions to the e-discovery process.\u003c/p\u003e","slug":"brittany-latour","email":"blatour@kslaw.com","phone":null,"matters":null,"taggings":{"tags":[],"meta_tags":[]},"expertise":[{"id":7,"guid":"7.capabilities","index":0,"source":"capabilities"},{"id":21,"guid":"21.capabilities","index":1,"source":"capabilities"},{"id":24,"guid":"24.capabilities","index":2,"source":"capabilities"},{"id":74,"guid":"74.capabilities","index":3,"source":"capabilities"}],"is_active":true,"last_name":"Latour","nick_name":"Britt","clerkships":[],"first_name":"Brittany","title_rank":9999,"updated_by":202,"law_schools":[{"id":1403,"meta":{"degree":"J.D.","honors":"","is_law_school":"1","graduation_date":null},"order":1,"pin_order":null,"pin_expiration":null}],"middle_name":" ","name_suffix":"","recognitions":null,"linked_in_url":null,"seodescription":null,"primary_title_id":84,"translated_fields":{"en":{"bio":"\u003cp\u003eBritt Latour is a Senior Staff Attorney in the Products Liability and Mass Torts Practice Group. Britt comes to the firm with a background in healthcare compliance and government investigations. She works closely with in-house counsel, outside counsel and vendors to develop and execute project plans for each stage of the Electronic Discovery Reference Model (EDRM) including identification, preservation, collection, review, and production of documents in complex litigation or government investigations. She collaborates with technology providers to leverage advanced tools to offer cost-effective and timely solutions to the e-discovery process.\u003c/p\u003e"},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":12276}]},"capability_group_id":3},"created_at":"2026-01-20T22:02:12.000Z","updated_at":"2026-01-20T22:02:12.000Z","searchable_text":"Latour{{ FIELD }}Britt Latour is a Senior Staff Attorney in the Products Liability and Mass Torts Practice Group. Britt comes to the firm with a background in healthcare compliance and government investigations. She works closely with in-house counsel, outside counsel and vendors to develop and execute project plans for each stage of the Electronic Discovery Reference Model (EDRM) including identification, preservation, collection, review, and production of documents in complex litigation or government investigations. She collaborates with technology providers to leverage advanced tools to offer cost-effective and timely solutions to the e-discovery process. Senior Attorney Auburn University  New York Law School New York Law School Auburn University  Florida North Carolina New York","searchable_name":"Brittany Latour (Britt)","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":427684,"version":1,"owner_type":"Person","owner_id":1533,"payload":{"bio":"\u003cp\u003eDr. Beverly Lorell is the Senior Medical and Policy Advisor with the firm\u0026rsquo;s FDA and Life Sciences Practice in Washington, D.C. Dr. Lorell specializes in the areas of clinical trial design of studies for drugs, devices and biologics; review of pre-market submissions; recalls; and assessment of matters involving a risk to health. She also specializes in the area of physician and industry relations and the development of independent scientific panels to advise health industries.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eDr. Lorell,\u0026nbsp;who was previously Professor of Medicine at Harvard University, has over twenty-five years of experience as a practicing interventional cardiologist and heart failure specialist. She is an internationally recognized clinical and basic science investigator with extensive experience in multi-center clinical trials and preclinical proof-of-concept translational science. Prior to joining King \u0026amp; Spalding, Dr. Lorell served as Vice President and global Chief Medical and Technology Officer at Guidant Corporation. There her responsibilities included evaluating emerging technologies and attendant regulatory challenges, determining product development priorities, and influencing clinical research strategies. She participated in the firm\u0026rsquo;s board for business development.\u003c/p\u003e\n\u003cp\u003eDuring her career at Harvard Medical School, she served the federal government in multiple roles including:\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eFood and Drug Administration\u0026rsquo;s Cardiovascular and Renal Drugs Advisory Committee. Notable issues included: Irbesartan (preservation of renal function in type 2 diabetes mellitus), Pravastatin/aspirin combination (can combination be justified based on meta-analysis in absence of specific trial data supporting the combination), Losartan (nephropathy in type 2 diabetes), Candesartan (blood pressure reduction in comparison with Losartan), Omapatrilat (balancing benefit of new antihypertensive vs risk of angioedema), Ranolazine - an antianginal, Alfuzosin- erectile dysfunction, and Verdenafil - prostatic hypertrophy (balancing drug benefits vs. risks of QT interval prolongation), Ximelagatran (balancing benefits of new antithrombotic vs. risks of hepatotoxicity),\u003c/li\u003e\n\u003cli\u003eFederally funded investigator of the National Institutes of Health,\u003c/li\u003e\n\u003cli\u003eNational task force and special emphasis panels of the National Institutes of Health, and\u003c/li\u003e\n\u003cli\u003eThe Cardiovascular Study Section of the National Heart, Lung, and Blood Institute of the National Institutes of Health.\u003c/li\u003e\n\u003c/ul\u003e\n\u003cp\u003eDr. Lorell\u0026nbsp;has served in national leadership positions in professional societies. She was an Established Investigator of the American Heart Association (AHA). Additional honors include election as Fellow of the American College of Cardiology (FACC) and the American Heart Association (FAHA) and founding member of the Heart Failure Society of America. She served on the Executive Committees of both the Council on Clinical Cardiology and the Council on Basic Science of the AHA. Recent national leadership roles included the national Executive Committee of the Task Force on Clinical Competence of the ACC, AHA and American College of Physicians, a body which determines national standards for medical competency for novel cardiovascular technologies. She was also a member of the Consensus Conference Group on Professionalism and Ethics of the ACC and AHA. She continues to be an active invited lecturer at national professional meetings, as well as Harvard Law School and Harvard Medical School.\u003c/p\u003e\n\u003cp\u003eShe now represents King \u0026amp; Spalding as a member of the Executive Committee of the New England Healthcare Institute, a nonprofit health policy organization, and as a member of the Steering Committee of the Clinical Trials Transformation Initiative, a public-private initiative between FDA, academic centers, and industry.\u003c/p\u003e\n\u003cp\u003eDr. Lorell\u0026nbsp;is a graduate of Stanford University, and she received her M.D. degree and her Residency in Internal Medicine from Stanford University Medical School. She received her advanced training as a Fellow in Cardiovascular Medicine at Harvard University. She is a Diplomate of the American Board of Internal Medicine, the Subspecialty Board of Cardiovascular Disease, and the Subspecialty Board of Interventional Cardiology. She is admitted to practice medicine in the states of California and Massachusetts. She is the author of over 160 medical science publications, 26 chapters and 2 books, including 8 recent publications in the area of health policy. Edward M. Basile, Partner at King \u0026amp; Spalding, and Dr. Lorell are authors of the recent publication, \u003cem\u003eThe Food and Drug Administration\u0026rsquo;s Regulation of Risk Disclosure for Implantable Cardioverter Defibrillators: Has Technology Outpaced the Agency\u0026rsquo;s Regulatory Framework?, \u003c/em\u003e61 FOOD AND DRUG LAW JOURNAL 251-272 (2006).\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eRecent Publications\u003c/strong\u003e\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eCo-author, \u003cem\u003eThe Food and Drug Administration\u0026rsquo;s Regulation of Risk Disclosure for Implantable Cardioverter Defibrillators: Has Technology Outpaced the Agency\u0026rsquo;s Regulatory Framework?, \u003c/em\u003e61 FOOD AND DRUG LAW JOURNAL 251-272 (2006)\u003c/li\u003e\n\u003c/ul\u003e\n\u003cp\u003e\u003cstrong\u003eMemberships\u003c/strong\u003e\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eEstablished Investigator of the American Heart Association (AHA)\u003c/li\u003e\n\u003cli\u003eFellow of the American College of Cardiology (FACC)\u003c/li\u003e\n\u003cli\u003eFellow of the American Heart Association (FAHA)\u003c/li\u003e\n\u003cli\u003eFounding Member of the Heart Failure Society of America\u003c/li\u003e\n\u003cli\u003eCouncil on Clinical Cardiology, Executive Committee\u003c/li\u003e\n\u003cli\u003eCouncil on Basic Science of the AHA, Executive Committee\u003c/li\u003e\n\u003cli\u003eExecutive Committee of the Task Force on Clinical Competence of the ACC, AHA and American College of Physicians\u003c/li\u003e\n\u003cli\u003eConsensus Conference Group on Professionalism and Ethics of the ACC and AHA\u003c/li\u003e\n\u003cli\u003eAmerican Board of Internal Medicine, Diplomate\u003c/li\u003e\n\u003cli\u003eSubspecialty Board of Cardiovascular Disease\u003c/li\u003e\n\u003cli\u003eSubspecialty Board of Interventional Cardiology\u003c/li\u003e\n\u003c/ul\u003e","slug":"bev-lorell","email":"blorell@kslaw.com","phone":null,"matters":null,"taggings":{"tags":[],"meta_tags":[]},"expertise":[{"id":23,"guid":"23.capabilities","index":0,"source":"capabilities"},{"id":81,"guid":"81.capabilities","index":1,"source":"capabilities"},{"id":103,"guid":"103.capabilities","index":2,"source":"capabilities"},{"id":21,"guid":"21.capabilities","index":3,"source":"capabilities"}],"is_active":true,"last_name":"Lorell","nick_name":"Beverly","clerkships":[],"first_name":"Bev","title_rank":9999,"updated_by":101,"law_schools":[],"middle_name":"H.","name_suffix":"M.D.","recognitions":null,"linked_in_url":null,"seodescription":null,"primary_title_id":11,"translated_fields":{"en":{"bio":"\u003cp\u003eDr. Beverly Lorell is the Senior Medical and Policy Advisor with the firm\u0026rsquo;s FDA and Life Sciences Practice in Washington, D.C. Dr. Lorell specializes in the areas of clinical trial design of studies for drugs, devices and biologics; review of pre-market submissions; recalls; and assessment of matters involving a risk to health. She also specializes in the area of physician and industry relations and the development of independent scientific panels to advise health industries.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eDr. Lorell,\u0026nbsp;who was previously Professor of Medicine at Harvard University, has over twenty-five years of experience as a practicing interventional cardiologist and heart failure specialist. She is an internationally recognized clinical and basic science investigator with extensive experience in multi-center clinical trials and preclinical proof-of-concept translational science. Prior to joining King \u0026amp; Spalding, Dr. Lorell served as Vice President and global Chief Medical and Technology Officer at Guidant Corporation. There her responsibilities included evaluating emerging technologies and attendant regulatory challenges, determining product development priorities, and influencing clinical research strategies. She participated in the firm\u0026rsquo;s board for business development.\u003c/p\u003e\n\u003cp\u003eDuring her career at Harvard Medical School, she served the federal government in multiple roles including:\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eFood and Drug Administration\u0026rsquo;s Cardiovascular and Renal Drugs Advisory Committee. Notable issues included: Irbesartan (preservation of renal function in type 2 diabetes mellitus), Pravastatin/aspirin combination (can combination be justified based on meta-analysis in absence of specific trial data supporting the combination), Losartan (nephropathy in type 2 diabetes), Candesartan (blood pressure reduction in comparison with Losartan), Omapatrilat (balancing benefit of new antihypertensive vs risk of angioedema), Ranolazine - an antianginal, Alfuzosin- erectile dysfunction, and Verdenafil - prostatic hypertrophy (balancing drug benefits vs. risks of QT interval prolongation), Ximelagatran (balancing benefits of new antithrombotic vs. risks of hepatotoxicity),\u003c/li\u003e\n\u003cli\u003eFederally funded investigator of the National Institutes of Health,\u003c/li\u003e\n\u003cli\u003eNational task force and special emphasis panels of the National Institutes of Health, and\u003c/li\u003e\n\u003cli\u003eThe Cardiovascular Study Section of the National Heart, Lung, and Blood Institute of the National Institutes of Health.\u003c/li\u003e\n\u003c/ul\u003e\n\u003cp\u003eDr. Lorell\u0026nbsp;has served in national leadership positions in professional societies. She was an Established Investigator of the American Heart Association (AHA). Additional honors include election as Fellow of the American College of Cardiology (FACC) and the American Heart Association (FAHA) and founding member of the Heart Failure Society of America. She served on the Executive Committees of both the Council on Clinical Cardiology and the Council on Basic Science of the AHA. Recent national leadership roles included the national Executive Committee of the Task Force on Clinical Competence of the ACC, AHA and American College of Physicians, a body which determines national standards for medical competency for novel cardiovascular technologies. She was also a member of the Consensus Conference Group on Professionalism and Ethics of the ACC and AHA. She continues to be an active invited lecturer at national professional meetings, as well as Harvard Law School and Harvard Medical School.\u003c/p\u003e\n\u003cp\u003eShe now represents King \u0026amp; Spalding as a member of the Executive Committee of the New England Healthcare Institute, a nonprofit health policy organization, and as a member of the Steering Committee of the Clinical Trials Transformation Initiative, a public-private initiative between FDA, academic centers, and industry.\u003c/p\u003e\n\u003cp\u003eDr. Lorell\u0026nbsp;is a graduate of Stanford University, and she received her M.D. degree and her Residency in Internal Medicine from Stanford University Medical School. She received her advanced training as a Fellow in Cardiovascular Medicine at Harvard University. She is a Diplomate of the American Board of Internal Medicine, the Subspecialty Board of Cardiovascular Disease, and the Subspecialty Board of Interventional Cardiology. She is admitted to practice medicine in the states of California and Massachusetts. She is the author of over 160 medical science publications, 26 chapters and 2 books, including 8 recent publications in the area of health policy. Edward M. Basile, Partner at King \u0026amp; Spalding, and Dr. Lorell are authors of the recent publication, \u003cem\u003eThe Food and Drug Administration\u0026rsquo;s Regulation of Risk Disclosure for Implantable Cardioverter Defibrillators: Has Technology Outpaced the Agency\u0026rsquo;s Regulatory Framework?, \u003c/em\u003e61 FOOD AND DRUG LAW JOURNAL 251-272 (2006).\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eRecent Publications\u003c/strong\u003e\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eCo-author, \u003cem\u003eThe Food and Drug Administration\u0026rsquo;s Regulation of Risk Disclosure for Implantable Cardioverter Defibrillators: Has Technology Outpaced the Agency\u0026rsquo;s Regulatory Framework?, \u003c/em\u003e61 FOOD AND DRUG LAW JOURNAL 251-272 (2006)\u003c/li\u003e\n\u003c/ul\u003e\n\u003cp\u003e\u003cstrong\u003eMemberships\u003c/strong\u003e\u003c/p\u003e\n\u003cul\u003e\n\u003cli\u003eEstablished Investigator of the American Heart Association (AHA)\u003c/li\u003e\n\u003cli\u003eFellow of the American College of Cardiology (FACC)\u003c/li\u003e\n\u003cli\u003eFellow of the American Heart Association (FAHA)\u003c/li\u003e\n\u003cli\u003eFounding Member of the Heart Failure Society of America\u003c/li\u003e\n\u003cli\u003eCouncil on Clinical Cardiology, Executive Committee\u003c/li\u003e\n\u003cli\u003eCouncil on Basic Science of the AHA, Executive Committee\u003c/li\u003e\n\u003cli\u003eExecutive Committee of the Task Force on Clinical Competence of the ACC, AHA and American College of Physicians\u003c/li\u003e\n\u003cli\u003eConsensus Conference Group on Professionalism and Ethics of the ACC and AHA\u003c/li\u003e\n\u003cli\u003eAmerican Board of Internal Medicine, Diplomate\u003c/li\u003e\n\u003cli\u003eSubspecialty Board of Cardiovascular Disease\u003c/li\u003e\n\u003cli\u003eSubspecialty Board of Interventional Cardiology\u003c/li\u003e\n\u003c/ul\u003e"},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":4352}]},"capability_group_id":2},"created_at":"2025-05-26T05:03:44.000Z","updated_at":"2025-05-26T05:03:44.000Z","searchable_text":"Lorell{{ FIELD }}Dr. Beverly Lorell is the Senior Medical and Policy Advisor with the firm’s FDA and Life Sciences Practice in Washington, D.C. Dr. Lorell specializes in the areas of clinical trial design of studies for drugs, devices and biologics; review of pre-market submissions; recalls; and assessment of matters involving a risk to health. She also specializes in the area of physician and industry relations and the development of independent scientific panels to advise health industries. \nDr. Lorell, who was previously Professor of Medicine at Harvard University, has over twenty-five years of experience as a practicing interventional cardiologist and heart failure specialist. She is an internationally recognized clinical and basic science investigator with extensive experience in multi-center clinical trials and preclinical proof-of-concept translational science. Prior to joining King \u0026amp; Spalding, Dr. Lorell served as Vice President and global Chief Medical and Technology Officer at Guidant Corporation. There her responsibilities included evaluating emerging technologies and attendant regulatory challenges, determining product development priorities, and influencing clinical research strategies. She participated in the firm’s board for business development.\nDuring her career at Harvard Medical School, she served the federal government in multiple roles including:\n\nFood and Drug Administration’s Cardiovascular and Renal Drugs Advisory Committee. Notable issues included: Irbesartan (preservation of renal function in type 2 diabetes mellitus), Pravastatin/aspirin combination (can combination be justified based on meta-analysis in absence of specific trial data supporting the combination), Losartan (nephropathy in type 2 diabetes), Candesartan (blood pressure reduction in comparison with Losartan), Omapatrilat (balancing benefit of new antihypertensive vs risk of angioedema), Ranolazine - an antianginal, Alfuzosin- erectile dysfunction, and Verdenafil - prostatic hypertrophy (balancing drug benefits vs. risks of QT interval prolongation), Ximelagatran (balancing benefits of new antithrombotic vs. risks of hepatotoxicity),\nFederally funded investigator of the National Institutes of Health,\nNational task force and special emphasis panels of the National Institutes of Health, and\nThe Cardiovascular Study Section of the National Heart, Lung, and Blood Institute of the National Institutes of Health.\n\nDr. Lorell has served in national leadership positions in professional societies. She was an Established Investigator of the American Heart Association (AHA). Additional honors include election as Fellow of the American College of Cardiology (FACC) and the American Heart Association (FAHA) and founding member of the Heart Failure Society of America. She served on the Executive Committees of both the Council on Clinical Cardiology and the Council on Basic Science of the AHA. Recent national leadership roles included the national Executive Committee of the Task Force on Clinical Competence of the ACC, AHA and American College of Physicians, a body which determines national standards for medical competency for novel cardiovascular technologies. She was also a member of the Consensus Conference Group on Professionalism and Ethics of the ACC and AHA. She continues to be an active invited lecturer at national professional meetings, as well as Harvard Law School and Harvard Medical School.\nShe now represents King \u0026amp; Spalding as a member of the Executive Committee of the New England Healthcare Institute, a nonprofit health policy organization, and as a member of the Steering Committee of the Clinical Trials Transformation Initiative, a public-private initiative between FDA, academic centers, and industry.\nDr. Lorell is a graduate of Stanford University, and she received her M.D. degree and her Residency in Internal Medicine from Stanford University Medical School. She received her advanced training as a Fellow in Cardiovascular Medicine at Harvard University. She is a Diplomate of the American Board of Internal Medicine, the Subspecialty Board of Cardiovascular Disease, and the Subspecialty Board of Interventional Cardiology. She is admitted to practice medicine in the states of California and Massachusetts. She is the author of over 160 medical science publications, 26 chapters and 2 books, including 8 recent publications in the area of health policy. Edward M. Basile, Partner at King \u0026amp; Spalding, and Dr. Lorell are authors of the recent publication, The Food and Drug Administration’s Regulation of Risk Disclosure for Implantable Cardioverter Defibrillators: Has Technology Outpaced the Agency’s Regulatory Framework?, 61 FOOD AND DRUG LAW JOURNAL 251-272 (2006).\nRecent Publications\n\nCo-author, The Food and Drug Administration’s Regulation of Risk Disclosure for Implantable Cardioverter Defibrillators: Has Technology Outpaced the Agency’s Regulatory Framework?, 61 FOOD AND DRUG LAW JOURNAL 251-272 (2006)\n\nMemberships\n\nEstablished Investigator of the American Heart Association (AHA)\nFellow of the American College of Cardiology (FACC)\nFellow of the American Heart Association (FAHA)\nFounding Member of the Heart Failure Society of America\nCouncil on Clinical Cardiology, Executive Committee\nCouncil on Basic Science of the AHA, Executive Committee\nExecutive Committee of the Task Force on Clinical Competence of the ACC, AHA and American College of Physicians\nConsensus Conference Group on Professionalism and Ethics of the ACC and AHA\nAmerican Board of Internal Medicine, Diplomate\nSubspecialty Board of Cardiovascular Disease\nSubspecialty Board of Interventional Cardiology\n Consultant Stanford University Stanford Law School Stanford University Stanford Law School","searchable_name":"Bev H. Lorell, M.D. (Beverly)","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":101,"capability_group_featured":null,"home_page_featured":null}]}}