Peter ANDRAWES

Peter Andrawes is a Quality/Regulatory Affairs Manager and PRRC with a PhD in Pharmacy. They currently oversee compliance for medical devices at Will Pharma, managing quality management systems and regulatory audits. Previously, Peter served as a Technical Referent at GMED, developing certification processes and training internal teams on compliance with EU regulations. They also held roles at various organizations, contributing to the certification and evaluation of medical devices while ensuring adherence to safety and performance standards. Peter's educational background includes a Master's degree in Pharmacy and ongoing doctoral studies at Université de Tours.