H. Srinath, MSc
Head - Q A & Regulatory
................................................................................................................
H. Srinath has over 25 years of experience in API manufacturing facilities. His last assignment was with Hikal Limited. He has worked in all the major departments such as Production, Quality Assurance and Regulatory affairs. He has been keenly involved in the preparation and filing of Drug Master File (DMF) for the US-FDA, EDQM, TGA - Australia, TDP-Canada and other European Regulatory authorities.
He was also the Management Representative for ISO certification programmes in his earlier tenure. Srinath joined Stellence in August 2009 and is in charge of Quality Assurance and Regulatory Affairs and has a team of four reporting to him.
