Durham Research Collaborative, LLC’s Post

First things first! Informed Consent is the first thing that should be obtained when enrolling a participant into a research study or clinical trial. Take care to not coerce or influence the participant to consent. This also means giving the participant enough time to consider whether they want to participate. You may give the potential participant a copy of the informed consent form (ICF) to take home to review and discuss with family, health care provider, or other trusted person before the screening visit. Please refer to E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1) section 4.8.7. || #clinicalresearch #ichgcp #cra #goodxpractice #goodclinicalpractice #clinicaltrials

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