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Document:USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998: Difference between revisions

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| [[Reference:USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998 -]] || HM || - || EN || FDA requires that an Institutional Review Board (IRB) review and have authority to approve, requiremodifications in, or disapprove all research activities covered by the IRB regulations [21 ...
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Latest revision as of 14:15, 16 July 2026


Document information
Reference USA FDA INFORMATION SHEET -

Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998

Validity area USA
Scope(s) HM
Document name FDA INFORMATION SHEET -

Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators

Version / Revision Jan-1998
Status Current
Document type Official recommendation
Language(s) EN
Description INFORMATION SHEET

Recruiting Study Subjects Guidance for Institutional Review Boards and Clinical Investigators

Official source Official link
Restricted access No
Submitted by Florian Adragna
Contributors

References

 ScopeDocument partLanguagePreview
USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998 -HM-ENFDA requires that an Institutional Review Board (IRB) review and have authority to approve, requiremodifications in, or disapprove all research activi…
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