VIMTA is the most reputed and No.1 choice in India for excellent quality clinical research services to Pharma, Biotech and Life-Science Industries. Our success is driven by our commitment to support customers win, through thorough understanding of the critical importance of time, technical on-time support, ethical care to subject safety, effective project management and strong GCP & GLP compliance.

We have rich experience, vast knowledge, advanced technologies and IT powered processes to conduct clinical studies. With strong local know-how and more than two decades of international regulatory experience VIMTA is your right partner for conducting clinical research studies in India.

Our expertise and leadership in Bioequivalence and Bioanalytical (BA/BE) Studies over the years has been extended to offer wider range of clinical research services such as clinical end point studies, claim studies for cosmetics and consumer care products, and clinical studies for complex neutraceuticals.

Regulatory Audits

Our Clinical and Bioanalytical sites are approved by CDSCO, Government of India

We have a very successful regulatory audit track record and have faced several regulatory audits from:

  • US FDA
  • WHO
  • MCC
  • DCGI
  • NPRA
  • UK MHRA and other European countries


  • Certificates

Central Lab Accreditations