Undoubtedly, the most critical roles in any clinical trial are the ones played by the investigators and site support staff. They’re the team that actually perform the activities leading up to or structuring an investigation of drug effects and safety. At Credevo.com, we strive to connect talented investigators and sites with new clinical trials requirements.
This helps in cutting down on the time and efforts for investigator identification and feasibility analysis. (You can assess feasibility for your clinical trial by posting your project summary here). Besides finding the investigators and sites, it’s also important to assess several other factors, like regulatory scenario, operational capabilities, resource availability and management, vendor search and management etc. Our blogs are humble attempts to address some of these areas. Feel free to explore, ask questions, share information or let us know if we could help in some way. Post your requirements, thoughts or messages to us below.
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