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.
Contacts
Capabilities
Suggested News & Insights
Animal Health, Nutrition & Technology Innovation – Shaping the Future of Animal HealthMonday, March 2, 2026 - Tuesday, March 3, 2026Sidley Represents Vivo Capital on Its Acquisition of Dutscher GroupFebruary 4, 2026Sidley Represents RoundTable Healthcare Partners in Its Partnership and Investment in ColorescienceFebruary 2, 2026Sidley Represents Simcere in €1 Billion Licensing and Collaboration Agreement With Boehringer IngelheimJanuary 29, 2025At the Table: Serving Up a Lively Discussion with the FDA, USDA, and HHSWednesday, January 28, 2026Medical Products Market Access: Favorable Advisory Opinion Reaffirms Discounting FlexibilitiesJanuary 21, 2026
- Stay Up To DateSubscribe to Sidley Publications
- Follow Sidley on Social MediaSocial Media Directory
