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Site-Management
Site Management Services from medpeace help take the burden off investigators planning to do clinical trials in India so that they can focus on the patient, and ensure that the study is conducted at the highest standards of quality, ethics and performance. This support ensures collection of high quality study data necessary for regulatory and product approval submissions. Continuous support to the study team and investigator during the study and make internal audit by independent audit to ensure best management services , Our proven comprehensive site support model involves placing a full-time, highly qualified clinical research coordinator(CRC) at each study site to assist the investigators and site staff with all day-to-day study conduct activities. The coordinators at our site management organization are trained to provide professional assistance to the investigator ensuring compliance with FDA, local regulatory and ICH-GCP guidelines and efficient completion of mandated tasks. Supported by an experienced project management team, the study coordinator can have a significant impact on the quality, ethics and performance of the site.
- Database of more than 75 registered Ethics Committee.
- The dedicated and well-trained research team.
- Work experience with several top pharmaceutical companies/CROs.
- Provide Site infrastructure.
- Assurance of delivering data on time.
- Patient recruitment strategies.
- Protection of patient's rights, safety & well-being.
- Rapid response to feasibility & start-up activities.
- Proper archival of all study materials at study completion.
- Quality Data Management.