Shweta Sharma is a regulatory affairs professional with expertise in medical device and biologics regulations. They have served as a Lead Engineer at HCL Technologies and as a Technical Data Associate at CDSCO (HQ) FDA, contributing significantly to regulatory analysis and compliance. Currently, Shweta holds roles as a Senior Regulatory Affairs Specialist and Regulatory Affairs Specialist in Canada, where they apply their extensive knowledge and BSI qualification as a Lead Auditor for ISO 13485, EU IVDR, and Health Canada. Previous experience also includes a position at bioLytical as a Regulatory Associate and a Senior Executive role at Biocon.
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