MedNous
Pharmacovigilance Is at a Crossroads
May 2025
The boundaries of medicine are rapidly changing. From gene editing to xenotransplantation, innovation is rapidly changing patient care as well as the requirements for drug safety, known as pharmacovigilance. Traditionally, pharmacovigilance has been directed towards the surveillance of drugs after they have been licensed for use. Going forward these rules will have to change.
This article was written by Ravi Patel, Senior Vice President, Global Patient Safety at United Therapeutics Corp and Anna Melin of Sidley and was originally published in MedNous (Managing European Medical Innovation), Vol 19, No 5, May 2025.
得意分野
Suggested News & Insights
Recharge & Recaffeinate With Sidley @ JPMMonday, January 11, 2027 – Tuesday, January 12, 2027GMP 2026: Regulatory Reliance, AI, and the Future of Pharmaceutical ManufacturingWednesday, December 2, 2026Sidley Represents Laza Medical in Its US$160 Million Series B Financing RoundNovember 4, 2026Sidley Represents Hanmi Pharm and Green Cross Biopharma in Licensing Agreement With BioMarinOctober 30, 2026U.S. Treasury Proposes Sweeping Limits on U.S. Investments in “Countries of Concern”: Biotechnology, Super Intelligence, and MoreOctober 28, 2026Sidley Represents Bolt Biotherapeutics in the Acquisition of Prana Therapies and Concurrent US$120 Million Private Placement FinancingOctober 26, 2026
- Stay Up To DateSubscribe to Sidley Publications
- Follow Sidley on Social MediaSocial Media Directory
