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Subscribe to: Posts (Atom). VM PHARMA GMP CONSULTANTS is based at Hyderabad and has been promoted by a seasoned, dynamic result oriented Ph.D professional with nearly 33 years of rich experience in the areas of Quality Assurance and Control, Regulatory Affairs, Process Development and design, Liaison and Coordination in Pharmaceutical industry (Both API and Finished dosage form). View my complete profile. Watermark template. Powered by Blogger.

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vvmpharmagmp | vvmpharmagmp.blogspot.com Reviews

https://vvmpharmagmp.blogspot.com

Subscribe to: Posts (Atom). VM PHARMA GMP CONSULTANTS is based at Hyderabad and has been promoted by a seasoned, dynamic result oriented Ph.D professional with nearly 33 years of rich experience in the areas of Quality Assurance and Control, Regulatory Affairs, Process Development and design, Liaison and Coordination in Pharmaceutical industry (Both API and Finished dosage form). View my complete profile. Watermark template. Powered by Blogger.

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vvmpharmagmp

Subscribe to: Posts (Atom). VM PHARMA GMP CONSULTANTS is based at Hyderabad and has been promoted by a seasoned, dynamic result oriented Ph.D professional with nearly 33 years of rich experience in the areas of Quality Assurance and Control, Regulatory Affairs, Process Development and design, Liaison and Coordination in Pharmaceutical industry (Both API and Finished dosage form). View my complete profile. Watermark template. Powered by Blogger.

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Ph : 91 99 4068 9600 Email : info@vvmpharmagmp.com. CGMP consultancy under one roof for design, implementation and the accreditation from USFDA, EDQM/MHRA, Australian-TGA, ANVISA, PMDA, MCC, ISO 9000, WHO GMP and other regulatory agencies. VVM Pharma GMP Consultants audited Divis Laboratories, Hyderabad facility for GMP compliance on behalf of its US client. VVM Pharma GMP Consultants conducted training on Basic Concepts of cGMP for the manufacture of Herbal and Ayurvedic Medicines (WHO-GMP).

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October 2nd, 2012. VM PHARMA GMP CONSULTANTS is based at Hyderabad and has been promoted by a seasoned, dynamic result oriented Ph.D professional with nearly 33 years of rich experience in the areas of Quality Assurance and Control, Regulatory Affairs, Process Development and design, Liaison and Coordination in Pharmaceutical industry (Both API and Finished dosage form). The promoter is also a IRCA (UK) certified Lead Auditor for ISO 9001.2008 QMS (Quality Management System).

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