Promotes Traditional Healthcare on Ethical Principles
Registration No. S/2L 25358 of 2014-2015
Registered under The W.B.Societies Act, 1961
For Manufacturers
For Manufacturers
Validate your research / projects through Independent Ethics Committee (CR) India
Best wishes for the season!
Clinical Research Trial has become an integral part of Pharmaceutical Companies and most of the Clinical trials in India are found to have deficiencies with ethics committees and have raised concerns about the quality of clinical research, timelines for regulatory approval and an unethical approach to the recruitment of trial subjects.
But we, at IEC (CR) India are committed to regulate and conduct scientific validation which is based on Ethical and Juridical aspects. The prime responsibility of IEC (CR) INDIA is to regulate clinical research, along with the government’s regulatory authority – The Drug Controller General of India (DCGI) / State DCs.
It is a matter of pleasure to communicate your good selves that, Independent Research Ethics Committee (CR) India is established in 2012 as per the guidelines from ICMR-GCP, to authenticate / validate trial projects / as well as to protect rights of trial participants.
As IEC (CR) India is the unique institute in the Eastern Zone, IEC (CR) India has tied up with CROs as well as Clinical Research Centers of AYUSH and Modern Medicine to provide maximum research facilities through single window system as per legal norms.
We are confident and very positive that you will definitely consider IEC (CR) India for the validation of your upcoming Clinical Research Validation.
