Sai K Reddy E

Sai k Reddy E is a Regulatory Affairs Specialist II at Zydus Pharmaceuticals (USA) Inc. since September 2022, with expertise in preparing regulatory filings, including 510(k) submissions and compliance with international regulations such as ISO 13485. Prior to this role, Sai k Reddy E served as Regulatory Affairs CMC Lead at Viant Medical, focusing on CMC technical writing and Annual Report submissions. At Dr. Reddy's Laboratories, responsibilities included reviewing and submitting DMFs in compliance with NMPA requirements. Sai k Reddy E holds a Bachelor's degree in Pharmacy from Jawaharlal Nehru Technological University and a Master's degree in Health Informatics from New England College.