Avacare offers custom solutions for clinical trials in India. Our passionate and experienced clinical trial experts accelerate delivery while maintaining the highest quality standards.
With more than 90 sites in India, the Avacare site network supports clinical development through the placement of highly trained clinical research coordinators at each research site dedicated to a specific protocol. Our research coordinators ensure each trial is conducted with the highest standards of quality, ethics and performance, offering a 95% patient retention rate.
With more than 90 sites in India, the Avacare site network supports clinical development through the placement of highly trained clinical research coordinators at each research site dedicated to a specific protocol. Our research coordinators ensure each trial is conducted with the highest standards of quality, ethics and performance, offering a 95% patient retention rate.
Our proven comprehensive site management model involves placing a full-time clinical research coordinator (CRC) at each study site to assist the investigators and site staff with all day-to-day study conduct activities. Our CRCs are trained to provide professional assistance to the investigator ensuring compliance with FDA, EMEA, local regulatory and ICH GCP guidelines. Supported by a centralized and experienced project management team, the CRC has a significant impact on the quality, ethics and performance of each site.
We also have comprehensive regulatory capabilities in India to navigate local regulatory requirements.
Presence at multispeciality and superspeciality sites in 24 cities.