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A Tale of Competing Cocaine Drugs: Genus Sues FDA Over its NCE ExclusivityRegulatory Affairs Professional SocietyWed, January 29th - 4:16 PM 2020
MHRA Offers Grace Period for Device Manufacturers Dealing With Withdrawn Notified BodiesRegulatory Affairs Professional SocietyWed, January 29th - 4:38 PM 2020
EU Regulatory Roundup: Pharmacists in 87% of EU Countries Report Drug Shortages got Worse in 2019Regulatory Affairs Professional SocietyThu, January 30th - 12:42 PM 2020
Recon: Eli Lilly Profit Boosted by Trulicity Demand; Roche Posts 2019 Growth Despite Biosimilar CompetitionRegulatory Affairs Professional SocietyThu, January 30th - 1:19 PM 2020
FDA Launches PEPFAR Drug DatabaseRegulatory Affairs Professional SocietyThu, January 30th - 2:49 PM 2020
2020 CDER Draft and Revised Guidance: What’s ComingRegulatory Affairs Professional SocietyThu, January 30th - 4:18 PM 2020
European Commission Calls for Observers to Join Annex XVI SubgroupRegulatory Affairs Professional SocietyThu, January 30th - 4:31 PM 2020
UK Explains What Happens to SPCs and Patents After the Brexit Transition PeriodRegulatory Affairs Professional SocietyThu, January 30th - 4:53 PM 2020
Hahn Stresses Importance of Data, RWE in First All-Hands MeetingRegulatory Affairs Professional SocietyThu, January 30th - 5:05 PM 2020
Regulatory Explainer: Everything You Need to Know About FDA’s Priority Review VouchersRegulatory Affairs Professional SocietyFri, January 31st - 9:47 AM 2020