Cosmos clinical trial echo-system offers a wide range of development techniques, including feasibility studies by continent, nation, and location, as well as clinical trial monitoring globally for all of your protocols, from simple to complex.
Our service team is client-focused, and we make every effort to deliver flexible, but timely, high-quality services.
Cosmos echo system provides end-to-end study operation capabilities to ensure that the research is completed successfully and on schedule.
Site Identifying
- Search engines from all across the world
- Handling CDA online with our 21 CRF Part 11 compliant eSignature capability.
Worldwide site viability
- Conducting clinical trial feasibility is critical for each clinical trial in order to evaluate clinical investigator and site skills, patient recruitment potential, deadlines, and many other factors in order to avoid clinical trial failures or delays. Cosmos delivers a very user-friendly and effective web-based platform for connecting with clinical investigators and sites all around the world. With just a few simple steps, you may connect with clinical investigators, run feasibility studies, review, and select.
What exactly is clinical trial feasibility?
Clinical trial feasibility is the process of determining the likelihood of conducting a specific clinical trial in a specific geographical region, also known as country level feasibility and site level feasibility, with the overall goal of achieving the best clinical trial completion in terms of timelines, targets, and costs.
Why should clinical trial feasibility be performed?
The majority of clinical trials fail owing to poor patient recruiting, ineffective clinical investigator selection, incorrect geographical preference, a lack of awareness of ethical and local regulatory issues, time delays, and other factors.
Conducting clinical trial feasibility reduces the costs paid as a result of incorrect assumptions and misinterpretations.
What should you anticipate from a clinical trial feasibility study?
After completing successful clinical trial feasibility, one should comprehend and forecast the investigator and site capabilities, patient recruiting potentials, region potential, regulatory timeframes, and overall timetable for study completion.
Cosmos makes conducting clinical trial feasibility extremely simple, with only a basic procedures. Sign up to establish your profile and post basic facts about your study; that’s all there is to it. You contact thousands of clinical investigators/sites/monitors/regulators.