Policy Guidance [by topics]
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OHRP welcomes comments on any of its policy guidances. Comments may be submitted to OHRP by email at: firstname.lastname@example.org (please insert the title of the specific guidance document in the subject field), or by mail to:
Division of Policy and Assurances
All relevant comments will be considered in OHRP decisions on timing and content of revisions to guidance documents, or development of new guidance documents. Comments generally will not result in direct responses from OHRP.
Adverse Events (see also Unanticipated Problems)
Biological Specimens (see also Coded Private Information)
Clinical Trial Websites (see also IRBs)
Coded Private Information (see also Biological Specimens)
Continuing Review [PDF - 52KB]
Informed Consent FAQ's [NEW]
IRB Registration FAQs
Repositories (see also Tissue Storage/Repositories)
Unanticipated Problems (see also Adverse Events)
Last revised: January 03, 2008