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Please note if HIPAA applies neither the participant nor their LAR should sign the HIPAA Authorization form. The information described in the IRB approved HIPAA Authorization form should be verbally communicated and oral authorization from the participant or LAR should be obtained. IRB Office Short Form Consent Template- English Version 11. 17. 2016 Connecticut Children s Medical Center Principal Investigator PI PI Phone Number Protocol Number Study Title Consent to Participate in Research...
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What is short form consent?
Short form consent is a shortened version of the standard consent form that still provides the necessary information and obtains the individual's permission.
Who is required to file short form consent?
Anyone seeking permission to use personal data in a limited and specific way may be required to file a short form consent.
How to fill out short form consent?
Short form consent can be filled out by providing concise information about the data being collected and the purpose for which it will be used, as well as obtaining the individual's signature or affirmation.
What is the purpose of short form consent?
The purpose of short form consent is to obtain permission from individuals to use their personal data in a clear and concise manner.
What information must be reported on short form consent?
Short form consent must report the specific data being collected, the purpose for which it will be used, and any additional information required by relevant regulations.
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