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Dr.Raghuveer is a renowned Scientist and Researcher with over 40 years of experience in Quality control ,Quality Assurance, Regulatory Affairs and Analytical Method development divisions of Pharma Industry.He has held various Senior managerial and Executive positions in Leading Pharma industries. Dr.Raghuveer's Pharma Consultants is the brain child of Dr.Raghuveer, a very senior executive in the Pharmaceutical Industry.
He holds Ph.D. degree in Pharmacy from Nagpur University and Master's degree in Medicinal Chemistry from Auburn University Auburn Alabama USA.
In his present position as a Consultant, he is involved in Advising Pharma Industries for their Quality Control, Quality Assurance,Regulatory and Analytical Method Development requirements.
Click here for an inside look at Dr' Raghuveer's Qualification, Experience and Research Publications.
CREDENTIALS
- Fellow of Royal Society of Chemists– CSci.,Cchem., FRSC (UK)
- Fellow of American Institute of Chemists (USA)
- Fellow Institute of Chemists(India)
- Life Member of Indian Pharmaceutical Association (IPA, India)
- Expert Member – Indian pharmacopoeial Commission, Govt. of India Anti-Retro-Viral Drugs
- Member of Technical Advisory Committee (Vaidya Vidhana Parishad), Ministry of Health, Govt of Andhra Pradesh – 1984-1990
- Examiner for M.Pharm (Pharmaceutical analysis), Nagpur University Nagpur India.
- Recognized Research Guide for M.Sc (Applied Chem) and Ph.D in Analytical Chem for JNTU, Hyd, India.
AWARDS
- Received Indian Drug Manufacturers association, award for Best Research paper published in 1992: Pharmaceutical Analysis
- Received Indian Drug Manufacturers association, award for Best Research paper published in 1982: Pharmaceutical Analysis
RESEARCH PUBLICATIONS
- A total of 51 research papers were published in National and International Journals on the pharmaceutical Analysis of Drugs and Pharmaceuticals.
- Presented Six scientific papers at various international and National Pharmaceutical Congresses.(list enclosed)
- Visited following countries for various Technical Discussions: United Kingdom,United States,Germany,Netherlands and China
PRESENT POSITION
- Consultant -- For Regulatory , Quality control and Quality Assurance Requirements of Pharmaceuticals in Pharma Industry.
- Provide Advice on the preparation of relevant SOP's, Regulatory Documentation like Preparation of Drug Master Files,Dossiers and QOS.
- Impurity profiling,Analytical method Development and Validations.
- Advise on Current Good Manufacturing Practices.
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ABOUT THE FOUNDER 
