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The Clinical Trials Scientific Review Committee (CT-SRC) is responsible for scientific review of clinical protocols, including: Scientific rationale. Study design. Appropriateness of biostatistical endpoints.
All projects must be approved by a Scientific Review Committee (SRC), and when necessary must also be approved by an Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and/or Institutional Biosafety Committee (IBC).
Scientists and engineers need to receive approval from a scientific review committee (SRC) and/or an institutional review board (IRB) before conducting experiments. This ensures that their investigations are safe and ethical.
A Scientific Review Committee (SRC) is a group of adults knowledgeable about regulations concerning experimentation especially with vertebrate animals and potentially hazardous biological agents. The SRC must review and approve all projects in these areas before experimentation may begin.
SRC also refers to the process of a project being reviewed. You may ask if a project requires SRC approval or if it has met SRC requirements. Projects involving humans are reviewed by a subcommittee of the SRC called the Institutional Review Board (IRB).
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All non-exempt microorganisms, cell lines, and tissues require SRC pre-approval, Form 6A and sometimes Form 6B. Culturing of microorganisms may NOT be conducted at home. (FTQ) All BSL-1 studies must be conducted at a BSL-1 facility or higher.

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