Help Center

Guides for investigators

You are responsible for the participants at your site. You review their data, assess adverse events, countersign consent and sign off visits and casebooks with your electronic signature.

Getting started

Account & sign-in

Study setup & team

eConsent

Participants

Data entry

Safety reporting

Queries, review & locks

Randomization & supplies

Trial management

Emails, texts & reminders

Troubleshooting

Guides for other roles

Still need help?

Email support@capture.study or use the contact form. Tell us the study name, what you were trying to do and the exact message on screen; a screenshot helps.

Please never send participant names, contact details or health information to support.