This is a requirement for studies meeting the definition of a clinical ... the RIT PI bears the responsibility of ensuring the requirement for posting of the consent form is met. For multi-site ...

The goal of the informed consent process is to ensure that the research subject is treated ... Upper-case text placed in brackets within this form gives contextual information about developing ...

The following forms and templates should be used to submit your research to the IRB ... not be retained in the final version. Use the Consent Document template to draft the consent form(s) for your ...

Note: The IRB must be provided with “sponsor verification” in the form of a letter signed by the sponsor(s) with the same wording given in the consent ... research use of their biological specimens ...

That is consent; it is not implied. Written and script forms of Information Sheets must be easy to read and/or understand, be in lay language that is suitable for the participant, and capture ...

The increase of remote and online research tools has increased the need for ... Researchers engaged in low-risk exempt studies may consider using verbal consent forms or verbal assent processes when ...

The following are some sample consent forms that you may use to guide the development of the consent forms that are most appropriate to your research study: Consent form for participation in ...