Value addition to our customers through our practical and logical Vision is our Mission

 

To support and assist the individual departments in the preparation of

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VVM 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 & Control, Regulatory Affairs, Process Development and design, Liaison & 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)

VVM Pharma GMP Consultants is specialised on the quality management of,

  • wide range of APIs but not limited to Beta- lactum antibiotics, Cephalosporins, Quinolones, anti-diabetics, analgesics, laxatives, anti-ulceratives and Steroids.
  • Various dosage forms like Tablets, Capsules, Syrups, Suspensions, Dry injectables, Liquid injectables, Ointments, Creams and Lotions
  • Lyophilisation and other sterile manufacturing activities of Active Pharmaceutical and dosage form industries.

VVM Pharma GMP Consultants has rich hands on experience in preparation and submission of DMFs/ANDAs and other dossiers to regulatory authorities and successful registration within the time frame.

The strength of VVM Pharma GMP Consultants lies in its involvement from the basic level to successful accomplishment of Regulatory inspections and thereafter continuous monitoring and support.