Transcription of Informed Consent Form Template for clinical trials
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Page 1 of 5 [Name of Principle Investigator] [ Informed Consent form for _____] Name the group of individuals for whom this Consent is written. Explanation Example [Name of Principal Investigator] [Name of Organization] [Name of Sponsor] [Name of Proposal and version] This Informed Consent form has two parts: Information Sheet (to share information about the research with you) Certificate of Consent (for signatures if you agree to take part) You will be given a copy of the full Informed Consent form PART I: Information Sheet Introduction Briefly state who you are and explain that you are inviting them to participate in the research you are doing.
Page 3 of 5 . If the protocol is for clinical research: Firstly, explain that there are standards/guidelines that will be followed for the treatment of their
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