Mark Thompson

Mark Thompson is an independent pharmaceutical & engineering consultant with over 30 years’ experience in GMP Quality Assurance within Sterile Product Manufacture. Mark has worked globally, satisfying many regulatory bodies to deliver process improvement, compliance, and innovation to the Pharmaceutical and Medical device industries.

Mark has contributed to training of several regulatory inspectorates around the world and his expertise lies in Project Management, CQV, Training and Consultancy services to the life science industries.

He is passionate about sharing his knowledge and best practices through publications, presentations, and training courses.