Dr.V.V.Ramireddy Joined MUPS after 22 years of Pharmaceutical Industry, India and USA. Most recently worked as the Global Technical Director of the National Chromatography Inco,. USA.

Dr.Ramireddy had to done more than 1200 Bioavailability and Bioequivalence studies and more than 800 bioanalytical methods were developed and validated by following the various regulatory guidelines. Dr.Ramireddy had vast experience in set-up the bioanalytical laboratories for small molecules as well as large molecules and involved set up bioanalytical laboratories at Aurobindo pharma, Alembic and Apotex Research Pvt Ltd.

Also had rich experience in facing GLP and GMP audits and clear the national and international audits i.e.USFDA, EMEA (Netherlands and AFSSAPS), ANVISA-Brazil, GCC and CDSCO.

Dr. Ramireddy had experience in quality control and led the quality control dept for 2yrs at Apotex Research Pvt Ltd.. During the tenure at Quality control Lab, implemented process optimization, capabilities enhancement, efficiency improvement program and cost optimization project were done using the lean tools. Also major audits i.e USFDA, MHRA and TGA were successfully cleared.

Dr. Ramireddy trained LC-MS/MS operation and bioanalytical sample preparation techniques like protein Precipitation, Liquid -Liquid extraction and Solid phase extraction for more than 200 people in the industry. He was participated and delivered a talk on New bioanalytical method validation which was organized by by Agilent, Bangalore, India in 2014.
Most recently I was participated and delivered a talk on “Introduction to Bioanalytics and Advances in Bioanalytics at Asia Pacific Pharmaceutical Science Summit forum at Shanghai China, Jan -19.