Sacha Lynch

Director Regulatory Affairs UK

Sacha has over 20 years of experience in European Regulatory Affairs with expertise spanning product development to post approval. Her educational background includes a degree in pharmacology and medical sciences, complemented by a master's in clinical research. Currently she is a Principal consultant with QbD Group, where she continues to support clients and leads project teams to develop robust strategies in their clinical development. Sacha actively contributes to the profession and leads the introductory course for TOPRA.

1 article

Regulatory AffairsClinical2026年4月13日 4 分钟

First-in-Human Operational Readiness for Emerging Biotechs: The Minimum Framework You Need

Prepare for First-in-Human trials with the right operational framework. Align safety, governance, and clinical execution to meet regulatory expectations.