Site Management is an important component of the entire human research. Too often companies fail to learn from their past mistakes and take the same approach to protocol development, trial planning and program execution. In order to overcome challenges in clinical trial planning, operations and site management our aim is to provide you clinical trial sites with state of the art technology, highest standards of quality and with the availability of skilled, GCP trained and experienced clinicians across varied therapeutic areas.
With decades of experience in the industry, we help you to speed up the site identification, qualification, initiation, and start up process. All our sites, mandatorily follow standard operating procedures which ensures ethical conduct of the trial and adherence to international and local standards of good clinical practice.
After extensive evaluations, we only recommend those sites which meet your study specific needs, helping you to significantly reduce the time and resources in trial conduct. We do contractual discussions in a centralised manner, which minimises the lengthy negotiations for each site.