Our services start with the right site selection. We understand that the success of the study can be influenced by the quality and reliability of the sites and the investigators.
We have an internal database of medical facilities for all major therapeutic areas. We can facilitate site selection for any OPD or IPD setting as well as government vs private medical facility.
We can facilitate the site using the site feasibility protocols short list of the best available sites commensurate with the requirements of the trials.
We can also facilitate the selection of investigators and the support staff based on the scope of the trials, experience, availability, infrastructure and recruitment potential.
We are responsible for the effective site monitoring, streamlining the performance of individual trials sites and ensure seamless communication between the various stakeholders throughout all stages of the clinical study.
We deliver operational and administrative support services to the clinical investigators at a research site.
We can anticipate and solve local challenges linked to the study protocol and risk mitigation.
