This template is essential for enrolling participants in clinical trials or research studies. It captures protocol details, participant ID, study arm, randomization information, visit type, investigator signature, and consent verification — ensuring regulatory compliance.
Protocol number, study title, PI details
Participant demographic information
Randomization and study arm assignments
Consent date & witness (if applicable)
Visit type (screening, baseline, follow-up, end-of-study)
Clinical research units, academic hospitals, CROs, trial investigators.
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