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Medical research / Clinical research / Clinical research ethics / Pharmaceutical industry / Medical ethics / Design of experiments / Title 1 of the Code of Federal Regulations / Clinical trial / Health Insurance Portability and Accountability Act / Informed consent


Informed consent information should be consistent with procedures, etc. as described in eProtocol application VA research: Refer to CHK-7 VA Research and AID-27m Reviewing VA Research for additional requirements Regul
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Document Date: 2014-08-06 19:30:22


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