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QA3 Form 1572 - PhRMA

Q7 form 1572 form 1572 A7 Statement of Investigator( form 1572) 21 CFR Part 312 Investigational New Drug Applications Investigator IRB FDA form 1572 2 1 Investigator IRB 1 Investigator FDA form 1572 FDA form 1572 FDA Form1572 FDA form

Clinical Practice Consolidated Guidance(ICH-GCP)に従う必要がありますが、たとえ各国の規制あ るいは ICH GCP に 従う場合であっても、FDA に提出された IND に含まれている以上、Investigator は 21CFR Part 312 の IND 要求事項にも様に従うよう FDA より求められています。

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  Form, Guidance, Clinical, 2517, Form 1572

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