Peter Andrawes

Peter Andrawes is a seasoned professional in the medical device industry, currently serving as a Medical Device Expert at ProductLife Group and as a Quality/Regulatory Affairs Manager and PRRC at Will Pharma since February 2024. With a strong background in compliance, Peter has held several key positions, including Product Reviewer at GMED, where responsibilities encompassed ensuring compliance with EU Regulation 2017/745, and Technical Referent for Article 117 of the same regulation, where guidelines for manufacturers were developed. Peter's career includes project management for certification related to CE marking and quality system certification and experience in regulatory affairs and logistics optimization in healthcare settings. Educational credentials include a Master's degree in Pharmacy from Université de Tours, obtained from 2012 to 2018.