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Safety biosafety committee

An Institutional Review Board (IRB) and an Institutional Biosafety Committee (IBC) must approve each gene therapy clinical trial before it can be carried out. An IRB is a committee of scientific and medical advisors and consumers that reviews all research within an institution. An IBC is a group that reviews and approves an institution s potentially hazardous research studies. Multiple levels of evaluation and oversight ensure that safety concerns are a top priority in the planning and carrying out of gene therapy research. [Pg.46]

Institutional Biosafety Committee) if the institution (i) conducts recombinant DNA research at Biosafety Level(BL) 3 or BL4, or (ii) engages in large scale (greater than 10 liters) research. The Biological Safety Officer carries out the duties specified in Section IV-B-3. [Pg.672]

V. Section IV-B-3-c-(5). Providing technicaladvicetoPrincipalInvestigators and the Institutional Biosafety Committee on research safety procedures. [Pg.676]

See other pages where Safety biosafety committee is mentioned: [Pg.6]    [Pg.93]    [Pg.228]    [Pg.259]    [Pg.660]    [Pg.671]    [Pg.673]    [Pg.673]    [Pg.674]    [Pg.674]    [Pg.676]    [Pg.676]    [Pg.676]    [Pg.680]    [Pg.286]    [Pg.50]    [Pg.498]   
See also in sourсe #XX -- [ Pg.137 , Pg.295 ]



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Safety committees Committee

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