History

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Preamble

  • Promoted by techno commercial persons having 25 years of Quality Systems and Research Experience
  • Promoters having experience in USFDA, UKMHRA, South Africa MCC, WHO GMP accreditation
  • Set up in 2002 with 4000 sq. feet rented place.
  • Shifted in 2006 to an independent building with 12000 sq. feet area.
  • In 2011 Acquired additional separate building with 10000 sq. feet, dedicated for human Bioequivalence/Bioavailability centre and Clinical Trials Phase II to Phase IV.

History - Landmark Information

  • 2002 Established in May 2002 at Govandi as a Public Testing Laboratory.
  • 2003 Approved by DCGI for conducting BA/BE Studies.
  • 2006 Relocation of facility to Pawane, Navi Mumbai. Approved by DCGI for conducting BA/BE studies at this Centre.
  • 2011 Relocation of BA/BE activities and Clinical Research at Turbhe. Approved by DCGI for conducting BA/BE studies at this Centre.
  • 2020 Approved by USFDA as a CRO for clinical research.

 

Our Vision

To maintain the highest degree of Analytical Excellence, state of the art instrumentation, quality standards and drug development services to esteemed customers.

Our Mission

To assist our customers in achieving newer goals by providing efficient & cost effective quality.