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Home  ::  Manufacturing  ::  Indrad Plant  ::  Compliances  
 

 

Torrent’s manufacturing facilities at Indrad meet cGMP guidelines and comply with WHO, USFDA, cGMP, MHRA and TGA norms amongst others.

Regulatory Approvals :

The Finished Dose Formulation facility at Indrad, Gujarat (India) caters to the growing demand for exports of branded generic products. The facility has been approved by following regulatory authorities:

  • FDA (USA)
  • BFARM (Germany)
  • ANVISA (BRAZIL)
  • Ministry of Health, (UAE)
  • TGA (Australia)
  • Ukraine Drugs Authority, (Ukraine)
  • National Drug Authority, (Uganda)
  • Pharmacy and Poison Board (Kenya)
  • Medicinal Control Authority of Zimbabwe, (Zimbabwe )
  • Gulf Cooperation council, (Gulf Countries)
  • ANMAT, (Argentina)
  • GMP, (Canada)
  • MHRA (UK)
  • MCC, (South Africa)
  • INVIMA (Columbia)
  • FDA (TANZANIA)
  • BFDA (TAIWAN)
  • FDA (KOREA)
  • NAFDAC (NIGERIA)

Quality Certifications :

  • Health, Safety (ISO-18001-2007)
  • Environment System( ISO-14001-2004)
  • Quality System Management (ISO 9001-2008)
  • Energy Management System (ISO 50001-2011)
  • 5 Star rating and Sword of Honor Award by British Safety Council
The Active Pharmaceutical Ingredient (API) manufacturing plant at Indrad (Gujarat, India) has been approved by European authorities.



 
 
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