Clinical Trial Feasibility At Your Fingertips
Easy, Quick and Credible

Find clinical trials, investigators and sites worldwide online. Perform feasibility super easily using automated processes.

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What is Credevo?

Credevo is an online management platform for clinical research.

Credevo helps investigators connect with trial managers worldwide at the click of a button. This way, investigators can conveniently find clinical trials of their interest and participate in their feasibility.

For trial managers, Credevo offers a wonderful solution to conduct feasibility with investigators globally, conveniently and super quickly.

Whom is Credevo for?

Investigators / Sites

Are you looking for clinical trials to work upon? Get convenient access to global and country-specific clinical trials and participate, or help your investigators participate, in their feasibility online.

Find Clinical Trials

Trial Managers

Are you looking for investigators in a new region, therapeutic segment or just another new trial? Reach thousands of investigators with introductory details of your clinical trial and perform feasibility online with interested investigators.

Find Investigators

Service Providers

Do you want to offer your services in monitoring, project management, shipment, regulatory or any other segment in clinical trials? Set up your service profile and get easy access to new business opportunities in clinical trials requiring them.

Find Opportunities

Explore the fastest growing database of investigators and sites


Research Sites


How can Credevo help you?

It connects you with trial managers, investigators and sites globally and helps you assess feasibility to perform clinical trials.

Connect and collaborate

Be a part of the network and get in loop with some of the most renowned clinical researchers.

Explore prospects to work on leading clinical development programs and give a high to your clinical research credentials, or work with diversely experienced investigators for your clinical trials and bring a phenomenal difference to recruitment scenario.

Standard process, with automation

Utilize standard clinical research systems and processes, while enjoying optimization in speed and quality brought by automation.

Ensure compliance with best documentation practices without actually spending too much time in them; and work smoothly without any repetitiveness or redundancy in the system.

Confidentiality and Control of data

Share your profile or clinical trial information only with those that you'd like to.

Take advantage of built-in non-disclosure terms or bring your own terms into play to ensure your data remains secure at hands of partners.

Optionally, perform feasibility using premium plans and restrict even the introductory information to only those that you search and select.

Corporate Plan Promotions

Get better prices, when signing up in Corporate Plans