The establishment of a Europe-wide system for verifying the authenticity of medicinal products is being held up by problems at EU member state level, particularly differences in national requirements regarding the new safety features that manufacturers must place on product packs from February next year.
Medicines for Europe, which represents manufacturers of generic and biosimilar medicines and is one of the stakeholders in the system,...
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?