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.