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Guiding Principles of Good AI Practice in Drug Development: What Every Regulatory Professional Needs to Know
In January 2026, the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) jointly published one of the most significant regulatory science documents in recent memory: Guiding Principles of Good AI Practice in Drug Development. For the first time, the world's two most influential regulatory authorities have aligned on a shared framework governing how artificial intelligence must be developed, validated, documented, and managed across the entire pharm
Jul 912 min read
From Hospital Pharmacy to the MHRA: How Jas Changed Her Career in Regulatory Affairs
Part of the Entry to Regulatory Success Stories Series Jas was a hospital pharmacist who felt stuck — until she discovered regulatory affairs. Here's how she made the leap to the MHRA, and what her journey can teach you. She Knew Medicines Inside Out. But the Industry Didn't Know Her. Jas had built her career in hospital pharmacy. Day after day, she worked at the intersection of medicines, patients, and clinical decision-making — reviewing prescriptions, counselling patie
Jun 198 min read
From Cosmetics to Pharma in 2 Months: How One Regulatory Professional Closed the Experience Gap
Part of the Entry to Regulatory Success Stories Series Edite had years of regulatory experience in cosmetics — but that wasn't enough to break into OTC and pharmaceutical roles. This is the story of how structured training transformed her application, secured her a role at a skin health company spanning OTC, pharma, and cosmetics, and set her on a clear path to career growth. If you're facing the same wall, read on. The Experience Gap That Holds Regulatory Professionals Back
Jun 197 min read