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Informed Consent/HIPAA Authorization Obtained: CRF Wisconsin Madison

- 11/17/16 - 1 form, 5 itemgroups, 21 items, 1 language

Itemgroups: Header, Informed Consent/HIPAA Authorized Obtained, Document(s) signed, undefined itemgroup, Informed Consent Refused

ODM Form derived from: https://ictr.wisc.edu/CaseReptTempt. Template Name: Informed Consent/HIPAA Authorization Obtained. Case Report Form (CRF)/Source Document templates were created for University of Wisconsin-Madison researchers. These templates are consistent with the FDA's CDASH (Clinical Data Acquisition Standards Harmonization) standards. The CDASH standards identify those elements that should be captured on a Case Report Form (CRF). The forms serve only as templates, and must be edited to meet the study data collection needs as described in the protocol.

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