We have a team of experts in
Site Managament
A regulated protocol is followed during a clinical trial, which is a subset of clinical research. The main purpose of clinical trials is to gather information about the safety and efficacy of newly developed drugs. For the medicine to be further approved and put on the market, clinical trial data is necessary.
We have established a strong track record of bringing diagnostics and treatments to market owing to our cutting-edge facilities and global network of investigators. India accounts for 18% of global disease burden but fewer than 2% of global clinical trials. The dearth of Clinical Trial Sites is one of the main causes of this phenomenon.
Indoriv Clinical wants to become the first of its kind nation-wide organized site management company offering one stop solution to CROs and Pharma companies.
Our exposure in clinical trials :
- Passed USFDA audits with no findings in Form 483
- Passed DCGI audit 2017, 2018 & 2019 with no major findings in all our sites
- Conducted more than 300+ clinical trials
- Worked with clients in the U.S. and Europe
