Key BIOS facts and Figures – 2025

Proposals to Accelerate the EU Integration of the Ukrainian Pharmaceutical Industry

(Short version) Critical Medicines Act: delivering a secure supply of critical medicines and active pharmaceutical ingredients in Europe

Position Papers on Electronic Product Information (ePI)

Streamlining Biosimilar Development: Key Aspects

Market Access Barriers: An overview of key barriers to generic and biosimilar market entry in select EU trading partners

Position Paper on the Overreliance on imports of Active Pharmaceutical Ingredients (APIs)

European Critical Medicines Act

Critical Medicines Act: delivering a secure supply of critical medicines and active pharmaceutical ingredients in Europe

Review of the SPC Manufacturing Waiver: a 2024 Industry Report

The Supplementary Protection Certificate (SPC) Manufacturing Waiver Regulation is applicable since 2 July 2022. The SPC Waiver has been introduced with the objective to remove the competitive disadvantage that European manufacturers of generic and biosimilar medicines are facing vis-à-vis third countries’ manufacturers, which can start manufacturing generics and biosimilars earlier due to shorter IP protection periods.

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