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Medicines for Europe

Combating Bioequivalence Data Fraud: Indian CROs Face Mandatory Registration

As Indian CROs are bracing for new registration mandates, an expert panel at the IGBA’s 3rd Bioequivalence conference discusses the implications of non-compliance in bioequivalence studies.

In Discussion With Medicines For Europe: The Year Of The Critical Medicines Act And Pharma Legislation Review

2025 is likely to be a game-changing year for the pharmaceutical industry. Generics Bulletin sat down with Medicines for Europe’s Adrian van den Hoven and Beata Stepniewska to discuss the opportunities of the Critical Medicines Act and EU pharmaceutical legislation revision.