Siva Vaithiyalingam

Siva Vaithiyalingam holds extensive experience in regulatory affairs within the pharmaceutical industry, currently serving as Senior Vice President of Regulatory Affairs at Cipla LTD since May 2016. Responsibilities include overseeing pre and post-approval regulatory strategies and filings for new drug applications and complex generics aimed at US FDA approvals. Previous roles encompass Principal at ARK Pharma Services LLC, Director of Regulatory Affairs at Teva Pharmaceuticals, and Senior Quality Reviewer at the FDA, where contributions involved ensuring the approval of ANDAs and leading quality initiatives. Siva's career began as a Senior Formulation and Process Development Scientist at Barr Laboratories and also included an internship in preformulation at Bristol-Myers Squibb. Siva holds a Ph.D. in Pharmaceutical Sciences from Texas Tech University Health Sciences Center, an M.Pharm in Pharmaceutics from the Indian Institute of Technology (Banaras Hindu University), and a B.Pharm in Pharmacy from Madurai Medical College.