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Good Clinical Practice (GCP) Guidelines - Home | OFFICE.doc

The objective of the ICH GCP guidance is to provide a unified standard for the European Union, Japan, ... (See Good Clinical Practice (GCP) Guidelines ...  Down

GUIDELINE FOR GOOD CLINICAL PRACTICE -.doc

ICH Harmonised Tripartite Guideline. Guideline for Good Clinical Practice. E6(R1) Current Step 4 version. dated 10 June 1996 (including the Post Step 4 corrections) ...  Down

Informed Consent Process - The University of Tennessee.doc

Informed Consent Form and Process. ... Refer to the ICH GCP E6 Guidelines and document the procedures of the Informed Consent Process: ...   Down

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  • Informed Consent Process - The University of Tennessee ...

    Informed Consent Form and Process. ... Refer to the ICH GCP E6 Guidelines and document the procedures of the Informed Consent Process:

    www.uthsc.edu/research/research_compliance/OHSP/docs/Reflections...
  • Microsoft Word - guidelines_for_amending_a_protocol.doc

    The purpose of this policy is to outline the additional requirements for compliance with ICH-GCP Guidelines in addition to those requirements described in NYU’s ...

    webdoc.nyumc.org/nyumc_d6/files/irb2/guidance.how_.to_.good...
  • Harmonized Good Clinical Practice (GCP) Guidelines for ...

    In the ICH GCP guideline the expression Regulatory Authorities includes the authorities ... Harmonized Good Clinical Practice (GCP) Guidelines for AVAREF countries ...

    https://www.healthresearchweb.org/files/AVAREFGCPGuidelinev0_1.docx
  • www.research.umn.edu

    Good Clinical Practice E6 (ICH-GCP E6) guidelines . for all research, only. to the extent that they are compatible with FDA and . DHHS regulations. The IRB will .

    www.research.umn.edu/.../ICH-GCP_E6_Guidance.docx