SQA Regulatory Surveillance Summary for Q2 2025 | Pharmaceutical Regulatory News

Regulatory Surveillance Summary for Quarter 2, 2025, featuring laboratory equipment imagery and listing global health authorities including ANVISA, FDA, EMA, NMPA, Health Canada, MHRA, WHO, and ICH.

This edition of the pharmaceutical regulatory news summary highlights key global developments impacting pharmaceuticals, medical devices, and compliance. The update covers enforcement actions, safety alerts, and regulatory guidance issued by major health authorities including ANVISA, FDA, EMA, NMPA, MHRA, Health Canada, WHO, and others, offering timely insight into evolving regulatory expectations worldwide.

SQA Regulatory Surveillance Summary | July 2020

By Laurel Hacche and Debra Cortner, SQA Associates European Medicines Agenda (EMA) Parenteral Drug Association (PDA) News – EMA: Final Assessment Report on Nitrosamines, 22 July 2020 The Committee for Medicinal Products for Human Use (CHMP) of the EMA published a final assessment report on nitrosamine impurities on 25 June 2020. The report calls on […]