The European Union’s Falsified Medicines Directive (FMD) has been in force since February 9, 2019, obliging pharmaceutical manufacturers to equip their products with so-called “safety features,” namely a unique identifier as well as an anti-tampering device. This webinar will:
- Include a step-by-step review of the FMD’s new obligations for pharmaceutical manufacturers.
- Provide guidance on safety feature verification by wholesalers, pharmacies, and hospitals and introduce the new repositories system.
- Contain discussion of some hot topics regarding the implementation of the safety features, including the responsibilities in case of parallel imports and the provisions of “FMD Hospital Pharmacy Services.”
Tuesday, March 26, 2019
12:00 P.M. – 1:00 P.M. ET
CLE credit will be applied for in CA, GA, IL, NY, TX and, if needed, NC and VA. Attendees will receive a Uniform Certificate of Attendance via email approximately 30 days after the program to seek CLE credit in other jurisdictions. New York lawyers: This program is considered transitional and non-transitional in content. The interactive webinar format is synchronous and approved for all lawyers. King & Spalding LLP / 1180 Peachtree Street, Atlanta, GA 30309 | CA Provider # 10947.
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If you have questions concerning this roundtable webinar, email firstname.lastname@example.org.