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Get the free EFS Master Clinical Trial Agreement (MCTA) - MDIC

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EFS MASTER CLINICAL TRIAL AGREEMENT IMPORTANT NOTE: This Early Feasibility Trial (EFS) Master Clinical Trial Agreement template is provided by The Medical Device Innovation Consortium (MDC) as an
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Who needs efs master clinical trial?

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Researchers and organizations conducting clinical trials
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Medical professionals and institutions involved in clinical research
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Pharmaceutical companies developing new drugs
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EFS Master Clinical Trial is a system for filing and managing clinical trials for new drugs or medical devices.
Any pharmaceutical company or medical device manufacturer conducting a clinical trial is required to file EFS Master Clinical Trial.
To fill out EFS Master Clinical Trial, one needs to provide detailed information about the trial protocol, study design, participant recruitment criteria, and safety monitoring procedures.
The purpose of EFS Master Clinical Trial is to ensure transparency and oversight in the conduct of clinical trials, and to facilitate the review and approval process by regulatory authorities.
Information that must be reported on EFS Master Clinical Trial includes study objectives, interventions, outcomes, adverse events, and data analysis plan.
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