Pratik Chavan

Pratik Chavan is a Medical Device Quality & Regulatory Consultant with extensive experience in regulatory affairs and quality management. Following a role as Director at Trupti Enterprises Ltd from 2009 to 2013, they served in various positions, including Quality Assurance Manager at GBUK Group (2016-2018) and Regulatory Affairs Specialist at BD (2019-2022). Currently, Pratik is a Senior Regulatory Affairs Specialist at Baxter International Inc. and has previously held roles such as Principal Regulatory Affairs Specialist at CooperVision and Quality & Regulatory Affairs Manager at CliniMed Ltd. Pratik earned a Master of Engineering in Biomedical/Medical Engineering from Queen Mary, U. of London, and completed A levels in Biology, Chemistry, and Maths at Lampton School.