Notebiva
Consent guides
Three guides for reading, understanding and questioning a consent form.
Where to begin
Three ways in
- I
New to the idea
Start with consent in plain words: what it means and how the discussion should go.
- II
Want to know where you stand
The rights guide lists what every participant keeps, from screening to the last visit.
- III
Holding a form now
The section-by-section guide explains what each part of the form should tell you.
The collection
All consent guides
IConsentInformed consent, explained in plain wordsWhat informed consent means, the elements it must cover, how the discussion should go, and consent that continues.9 min readIIRightsYour rights as a clinical trial participantVoluntary participation, the right to leave, information, privacy, injury care, and who to contact with concerns.9 min readIIIThe formWhat a consent form covers, section by sectionThe key information page, purpose, procedures, risks, benefits, alternatives, costs, privacy and signatures.9 min read
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