The increasing prevalence of chronic diseases and emergence and outbreak of various infectious diseases has not only fuelled the demand for newer therapeutic categories and novel treatment options, but also created the need for better treatment options in existing therapeutic categories. Over the last few years, the segment has seen an upsurge due to rising number of biologics, increased R&D spending, and the demand for advanced technologies; all of which require specialized and focused clinical trials.
As the Pharmaceutical industry evolves constantly to keep pace with the changing market dynamics and regulatory compliances; we at VIMTA are equipped to provide you end-to-end services for all your clinical research development needs. Having an experience of more than three decades, we have been pioneers in India offering quality services for clinical trials and BA/BE requirement of Pharma, Biotechnology and Life Sciences Industries. Our proven scientific rigor, highly advanced instrumentation capabilities, and deep understanding of the various regulatory requirements & compliances enables us to curate customized clinical research solutions to suit your specific needs.
At VIMTA, we have successfully delivered projects across various therapeutic categories inclusive but not limited to
With experience and skills in diversified segments, we have successfully handled trials and BA/BE studies for complex molecules, inhalation dosage forms, patch studies, solid oral dosages, vitamins, hormones, topical applications, nutraceuticals and many more. We have also successfully undertaken trials for topical products and claim studies including skin irritation and skin sensitization; and have proven experience in niche areas such as complex studies involving female population, postmenopausal women, long housing studies, complex elemental analysis, and unconventional BA/BE studies to name a few
With VIMTA, you can be assured of stringent quality compliance at each stage of the trial process and have an in-house laboratory for pathology services, which is NABL and CAP accredited. At VIMTA, our strong regulatory track record has been a testimony to our quality compliance and we have been successfully audited by USFDA, EU, WHO, ANVISA, NRPA, MHRA and CDSCO.
At VIMTA, we fully understand the challenges you face, and are equipped to offer you the resources and scientific acumen needed for reliable and reproducible results. When you work with VIMTA, you are supporting a team with strong ethics and principles, a team that is dedicated to your success and the safety of the end user of your products.