Investigator's Registration & Guidelines for Clinical Research.

The party or investigator with a wish to conduct clinical trial in India has to first register himself in India. CRO-India guides investigator about the process and eligibility requirements for registration in India. A clinical trial investigator before registering himself to conduct trials must ensure that he abides by all compliance with the GCP guidelines and must be thorough with the use of investigational product as described in the standardized protocols. It's the duty of the investigator to ensure all medical care of the subject, as the   subject is wholly dependent on the investigator during the trials.

Investigator while registering has to agree all terms and conditions set by regulatory authorities for conducting clinical trials in India. India follows all the international compliance while it give license or registration for clinical trials. Thus it adds to the responsibility of investigator also that he meets all the standards by GCP-ICH guidelines.

To get detailed version of guidelines for clinical research in India, click on the following link:

An Insight into Good Clinical Practice

http://fermish.com/GCP/GCP_intro.htm