“Courtesy begins at home” and similarly the data of a clinical trial is generated at each of the participating sites in a study. The critical importance of an effective site management; be it by providing trained clinical study coordinators, or by delivering ongoing training; or by frequent reviewing of the study documents, is very well known to the clinical research fraternity.

We at Consortium Clinical Research, take up the immense responsibilities of the sponsors, partner with the chosen investigators and ensure that the integrity and credibility of data collected is assigned with very high percentage of adherences to the protocol, the documented SOPs and to the statutory requirements.