[Answer] ICH GCP guidelines do what?

Answer: set standards for the design conduct monitoring and reporting of clinical research

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ICH GCP guidelines do what? Difference Between Indian GCP & ICH-GCP Genelife Clinical Research Pvt. Ltd.: Difference Between Indian GCP & IC… ICH Guidelines Guidelines : ICH Are you ready for the ICH GCP E6 (R2) Addendum? - TCTC Group Good Documentation Practices - GMPTraining.com This International Conference on Harmonization ( ICH ) document makes recommendations on information that should be included in a core clinical study report of an individual study … ICH - GCP Guidelines for Clinical Trials The European Agency for the Evaluation of Medicinal Products (EMEA) The main task of the EMEA is to FDA Center for Drug Evaluation and Research … Guideline for good clinical practice E6(R2) EMA/CHMP/ ICH /135/1995 Page 6/68 Introduction Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing conducting recording and reporting t...

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