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FAQs on Externally Administered IBCs - NIH Office of Science Policy

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Can an institution that does not have an IBC use an externally administered IBC to review and approve research subject to the NIH Guidelines?

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Biosafety and Biosecurity Policy

osp.od.nih.gov › Policies

Companion Guide to U.S. government policies for oversight of DURC ... Externally Administered IBCs · IBC Meetings and ... 2 and IBC Requirements under the NIH ...

FAQs on Transgenic Animals... · Major Actions under Section III...

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FAQs on Institutional Biosafety Committee (IBC) Administration

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How do the NIH Guidelines apply to the containment or release of plants and animals containing recombinant or synthetic nucleic acid molecules (e.g. have ...

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NIH Office of Science Policy

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The NIH Office of Science Policy (OSP) works across the biomedical research enterprise to ensure NIH policy evolves in tandem with rapidly advancing science and ...

About Us · Biosafety and Biosecurity Policy · Policy Areas · FDA-NIH Resource on...

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[PDF] NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic ...

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https://osp.od.nih.gov. NIH OFFICE OF SCIENCE ... Section III-E-2-b or other sections of the NIH Guidelines. ... Biosafety Committee's response to the Office of ...

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FAQs About IBC Meetings and Minutes - NIH Office of Science Policy

osp.od.nih.gov › policies › faqs-about-ib...

Containment conditions to be implemented (biosafety level and any special provisions). In general, the IBC meeting minutes should offer sufficient detail about ...

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[PDF] United States Government Policy for Institutional Oversight of Life ...

www.phe.gov › durc-policy

Sep 24, 2014 · This Policy addresses dual use research risks holistically, that is, the risk that knowledge, information, products, or technologies generated.

Interim Laboratory Biosafety Guidance for Research with SARS-CoV-2 ...

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FAQs – Interim Laboratory Biosafety Guidance for Research with SARS-CoV-2 and IBC Requirements under the NIH Guidelines for Research Involving Recombinant or ...

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