Informed consent is one of the primary requirements of research involving human participants ... provided the conditions described on the waiver form are fulfilled.

The short form written consent process does not apply when: research is exempt ... the DHHS requirement for documentation of informed consent as codified at §46.117, item (c); or the investigators ...

But when a scientist takes a swab of your saliva, a sample ... Before any research can go ahead, a patient must complete a customised form. The way researchers get informed consent is guided ...

Informed consent is an agreement between the investigators and the research participants. A signed informed consent form notifies potential research ... You may use this sample tempate to get started.

Note: Always use lay language that is appropriate to the population being asked to sign the form. Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form ...