Pharmafile Logo

Search and browse hundreds of industry specific terms and phrases or suggest your own terms and definitions.

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W |

Informed consent document

A document which describes the rights of participants in a clinical study, as well as explaining details of the study. This includes the study’s purpose, duration, required procedures, and key contacts, while also outlining the risks and potential benefit.

See also:
Clinical trial
Eligibility criteria
Drop out
Trial endpoint

Subscribe to our email news alerts

Latest content

Latest intelligence

Quick links