Event format: In-person and Online Live Stream.
Location: Basel, Switzerland.
Dates: 20–21 October 2026.
Registration includes training materials, interactive workshops, case studies, networking opportunities, and a Certificate of Completion.
Designed for professionals in pharmaceuticals, biotechnology, biologics, medical devices, regulatory affairs, quality assurance, manufacturing, and product development.
Participants will gain practical knowledge of FDA regulations, EU MDR Article 117 requirements, design controls, risk management, regulatory submissions, and lifecycle management.
Early registration is recommended due to limited seating.
Online participants can attend all sessions remotely and interact live with the trainer and delegates.