Sonika Mehra

Sonika Mehra is a Post Market Surveillance Professional at Baxter with a Master’s degree in Biotechnology and seven years of experience in the biopharma and medical device industry. They have worked at Biocon Biologics and Zydus, holding positions that involved complaint handling, quality management system oversight, and authoring pivotal regulatory documents. Currently, Sonika focuses on the interpretation and evaluation of medical device quality complaints, ensuring compliance with regulatory standards. Their expertise includes audit planning, report preparation, and knowledge of FDA and ISO 13485 regulations.