药物临床试验理审查工作指导原则-EN.pdfVIP

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药物临床试验理审查工作指导原则-EN.pdf

药物临床试验理审查工作指导原则-EN

Translated by RDPAC For RDPAC Member Companies Use Only 6. the medical treatment and protection of the research participants; 7. privacy and confidentiality; and 8. the trials involvingvulnerable persons. Article 29 For the purpose of ensuring the quality of ethical review and its review meeting, the ethics committee should manage and control the quality of ethical review. The meeting of ethical review should be conducted following the stipulated procedure and agenda. Sufficient deliberation sh

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