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 | June 2020

By Laurel Hacche and Debra Cortner, SQA Associates United States Food and Drug Administration (US FDA) Guidances Patient-Focused Drug Development: Collecting Comprehensive and Representative Input, June 2020 US FDA is publishing a series of guidances (a total of four) intended to facilitate the advancement and use of systematic approaches to collect and use robust and […]