PDF-Informed Consent Information Sheet Guidance for IRBs Clinical Investigators and Sponsors PDF document

Comments and suggestions regarding this draft document should be subm itted within 60 days of publication in the Federal Register of the notice announcing the availability

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Published on 2014-11-10

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Informed Consent Information Sheet Guidance for IRBs Clinical Investigators and Sponsors: Transcript

PDF-Informed Consent Information Sheet Guidance for IRBs Clinical Investigators and Sponsors PDF document

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Informed Consent Information Sheet Guidance for IRBs Clinical Investigators and Sponsors: Transcript

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