Simrit Padda, MS, RAC, Regulatory Affairs Consultant 1
Simrit Padda, MS, RAC, has over 10 years of experience in delivering regulatory affairs support spanning multiple therapeutic areasfor prescription drugs, over-the-counter products, and biologics. Her proficiency includes adept preparation, management, and compilation of submissions for INDs/CTAs, NDAs/NDSs, Annual Reports, DMFs, and various regulatory filings for both FDA and Health Canada.
Simrit has experience writing and reviewing CMC documents for drug products and compiling CSRs for regulatory submissions. She collaborates with Electronic Publishing to guarantee submissions meet quality standards and comply with eCTD specifications.
