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The international council for harmonisation of technical requirements for pharmaceuticals for human use (ich) is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of pharmaceuticals and develop ich guidelines. Interpretation and application of ich e6 (r3) Sign in to the ich private platformemail address

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The ich q3e draft “guideline for extractables and leachables” and supporting document has reached step 2b of the ich process on 1 august 2025 and entered the step 3 public consultation period. The ich secretariat is pleased to announce the publication of the following training module, now available in the ich training library In the pharmaceutical sector, the principles and framework of ich q9, coupled with the official ich training material that supports this guideline, are instrumental in enhancing the application of effective quality risk management by industry and regulators.

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It includes the ich medical terminology (meddra), the common technical document (ctd) and the development of electronic standards for the transfer of regulatory information (estri).

This presentation is protected by copyright and may, with the exception of the ich logo, be used, reproduced, incorporated into other works, adapted, modified, translated or distributed under a public license provided that ich's copyright in the presentation is acknowledged at all times. The ich harmonised guideline was finalised under step 4 in february 2002 This document is intended to address recommendations on the application of bracketing and matrixing to stability studies conducted in accordance with principles outlined in the main stability guideline.