The European Medicines Agency, along with the heads of national competent authorities in the EU, has formed a new task force to establish a roadmap and issue recommendations on how drug regulators can use big data to “support research, innovation and robust medicines development”.
The task force, which is being chaired by the Danish Medicines Agency and co-chaired by the EMA, will look at,...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?