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ICH HARMONISED TRIPARTITE GUIDELINE. GOOD MANUFACTURING PRACTICE GUIDE FOR. ACTIVE PHARMACEUTICAL INGREDIENTS. Q7. Current Step 4 version. to 1995, such as the International Conference on Harmonization (ICH). Good Clinical Practice: Consolidated Guideline and is organized as a.ICH E6 (R2) Good clinical practice · Table of contents · Current version - Revision 2 · ICH: E 6 (R2): Guideline for good clinical practice - Step 5 (PDF/693.2 KB). The work carried out by ICH under the Efficacy heading is concerned with the design, conduct, safety and reporting of clinical trials.

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