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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Date: 2014-08-06 19:30:22 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 Add to Reading List Source URL: humansubjects.stanford.edu Download Document from Source Website File Size: 55,03 KB Share Document on Facebook

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