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Study Feasibility
Study feasibility is an initial step in the conduct of any clinical trial. Medpeace facilitates this initial step by a well organized, systematic and detailed process. The presence of Medpeace Clinical Research Coordinators in every city ensures that the data collection is real time and factual. The feasibility process includes the following: Initial receipt of study synopsis from the client
- 1. Medpeace internal review for the study specific requirements in terms of the site, type of patient pool, investigator experience and expertise, status of Ethics Committee, site infrastructure and many other parameters
- 2. Shortlisting of study requirements and the sites in the medpeace database
- 3. Scheduling appointments with shortlisted sites and investigators
- 4. Personally meet the investigators and discuss the study synopsis, their interest and willingness to take up the study, patient pool, referral activities and other logistics
- 5. Personal meet and/or telecon by medpeace people with investigators for discussions and clarification of queries, if any
- 6. Collate and compile site responses into a Site Feasibility Grid within timeline
- 7. Grade and prioritize select sites based upon a number of factors
- 8. Include study specific projections, timelines and Risk Evaluation and Mitigation Strategy