Informed Consent Form

Summarized by Plex Health
Last Updated: 04 May 2022

Get the most up to date public health information from CDC: https://www. coronavirus. gov Get the latest research info from NIH: https://covid19. nih. gov/ In a professional research study, the informed consent form is the file used during the informed consent procedure that is the basis for describing to prospective topics the prospective threats and benefits of a research study and the rights and responsibilities of the events included. The informed consent form in a scientific research requires Institutional Review Board testimonial and approval prior to the research study starts. In a registry, the informed consent is the paper that describes the legal rights of a registry participants and provides details about the registry, such as its objective, period, vital calls, and just how the registry data will be shared and used. Review by an IRB may be required if the registry information includes specific wellness or clinical info or if the registry data will be used in therapy advancement process, even if that is in the long run.

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