Generics Bulletin
HBW Insight
In Vivo
Medtech Insight
Pink Sheet
Scrip
Close
Search
Search
Generics Bulletin
HBW Insight
In Vivo
Medtech Insight
Pink Sheet
Scrip
Case Study: Pushing The EU’s IVD Regulation To Its Limits With Next Generation Sequencing
Oct 07 2025
•
By
Amanda Maxwell
The FDA often requires 15 years of postmarket follow-up for approved gene therapies.
(Shutterstock)
More from Regulation
More from Policy & Regulation