·         Code of federal regulations

·         FDA regulations

·         ICH guidelines for GCP

·         ICH clinical safety data management

·         Clinical Research Associate responsibilities


We provide training for candidate’s who are interested to gain knowledge and skill in application of the conduct of clinical investigation’s involving human’s in accordance with the international conference on harmonization guideline for GCP,the united states code of federal regulation’s (CFR) and ethical principles that guide clinical research consistent with the principle’s of the Nuremberg code, the Belmont report and deceleration of Helsinki.