To support and assist the individual departments in the preparation of 
Dr.V.Ramasubramanian has done doctorate degree(Ph.D) from Madras University under the able guidance of Dr.S.Narasimhan, a learned scientist in boron chemistry and a student of noble laurate H.C Brown
Dr V.Ramasubramanian has two valid patents and number of international publications to his credit..
He has also done IRCA(UK) Lead Auditor for ISO9001.2008 QMS
He has undergone specific cGMP (ICHQ7/EUGMP) training in Italy and Iceland
Dr. V.Ramasubramanian is having about 33 years rich experience in Pharmaceutical industries ( Both API and Finished Dosage Form),
He has worked in various reputed leading Pharma Companies which includes 4 hi-tech multinational companies namely,
- ICI (India) Ltd (UK based multinational company)
- Teva Pharmaceuticals (Israel based multinational company)
- Alchymars (Italy based multinational company)
- Actavis Pharmaceuicals (Iceland based multinational company)
Other leading Indian companies
- SOL Pharmaceuticals
- American Remedies
Dr. V.Ramasubramanian started his career as Chemist (Analytical &Process Development) in ICI (India)Ltd, Chennai and started learning and practising all the fundamentals of international quality system through his 11 years career in that company.
To develop his career further up, he preferred to work in other leading companies in various capacities and rose to a level of Vice President (QA/QC/RA) .
He had been heading QA/QC/RA (both API &Dosage form) for the last 20 years in various capacities and has practical hands on experience in design, implementation and the accreditation process from USFDA, EDQM/MHRA, Australian-TGA, ANVISA, PMDA, MCC, ISO 9000 and other regulatory agencies
He had also worked as a Corporate Auditor (Quality &Compliance, Asia Pacific) in Actavis and developed skill and rich experience in auditing API and Dosage industries both within India and abroad for quality system compliance as per ICH Q7/EUGMP and other regulatory standards
