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1 international conference ON harmonisation OF TECHNICAL REQUIREMENTS. FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE. ICH HARMONISED GUIDELINE . GUIDELINE FOR elemental impurities . Q3D. Current Step 4 version dated 16 December 2014. This GUIDELINE has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. At Step 4 of the Process the final draft is recommended for adoption to the regulatory bodies of the European Union, Switzerland, Japan, USA and Canada. Q3D. Document History Code History Date Q3D Approval by the Steering Committee under Step 2a. 6 June 2013.

2 Approval by the Steering Committee under Step 2b and 6 June Q3D. release for public consultation. 2013. Post sign-off corrigendum in: 14 June 2013. Table W and Al were removed from the list of included Q3D elemental impurities in Class 2B and 3 respectively. Table the Class for Ni was changed to read 3 instead of 2. Post sign-off minor editorial corrections including: removal of 26 July references to Appendix 5 (pgs i deletion of redundant 2013. text (pg 4); change of Option 2 to Option 2a (pg 10); insertion Q3D of omitted text under Safety Limiting Toxicity (pg 35);. removal of duplicated redundant text (pg 41); replacing references to metals in text and metal in Table title with elementals and elements (pg 73); and deletion of header Table (pg 75).)

3 Addition of line numbers to facilitate the provision of 30 September Q3D. comments by stakeholders. 2013. Approval by the Steering Committee under Step 4 and 12 November Q3D. recommendation for adoption to the ICH regulatory bodies. 2014. Current Step 4 version Code History Date Corrigendum to correct: the modifying factor in the text of the 16 December safety assessment for Selenium (changed to 2 instead of 10 2014. Q3D consistent with Section ); and two references for consistency in the safety assessments for Barium (deleted reference) and Vanadium (revised reference). Legal notice: This document is protected by copyright and may be used, reproduced, incorporated into other works, adapted, modified, translated or distributed under a public license provided that ICH's copyright in the document is acknowledged at all times.

4 In case of any adaption, modification or translation of the document, reasonable steps must be taken to clearly label, demarcate or otherwise identify that changes were made to or based on the original document. Any impression that the adaption, modification or translation of the original document is endorsed or sponsored by the ICH must be avoided. The document is provided "as is" without warranty of any kind. In no event shall the ICH or the authors of the original document be liable for any claim, damages or other liability arising from the use of the document. The above-mentioned permissions do not apply to content supplied by third parties. Therefore, for documents where the copyright vests in a third party, permission for reproduction must be obtained from this copyright holder.

5 GUIDELINE FOR elemental impurities . ICH HARMONISED GUIDELINE Having reached Step 4 of the ICH Process at the ICH Steering Committee meeting on 12 November 2014, this GUIDELINE is recommended for adoption to the regulatory parties to ICH. TABLE OF CONTENTS. 1. INTRODUCTION .. 1. 2. 1. 3. SAFETY ASSESSMENT OF POTENTIAL elemental impurities .. 1. Principles of the Safety Assessment of elemental impurities for Oral, Parenteral and Inhalation Routes of Administration ..1. Other Routes of Administration ..2. Justification for elemental Impurity Levels Higher than an Established PDE ..3. Parenteral Products ..4. 4. ELEMENT 4. 5. RISK ASSESSMENT AND CONTROL OF elemental impurities .

6 5. General Principles ..5. Potential Sources of elemental impurities ..5. Identification of Potential elemental impurities ..6. Recommendations for Elements to be Considered in the Risk Assessment ..7. Summary of Risk Assessment Process ..8. Special Considerations for Biotechnologically-Derived Products ..9. 6. CONTROL OF elemental impurities ..9. 7. CONVERTING BETWEEN PDES AND CONCENTRATION LIMITS ..10. 8. SPECIATION AND OTHER CONSIDERATIONS .. 12. 9. ANALYTICAL 12. 10. LIFECYCLE MANAGEMENT .. 12. GLOSSARY .. 13. 17. Appendix 1: Method for Establishing Exposure Limits .. 18. Appendix 2: Established PDEs for elemental impurities .. 21. Appendix 3: Individual Safety Assessments.

7 23. Appendix 4: Illustrative 68. GUIDELINE FOR elemental impurities . Q3D. 1. INTRODUCTION. elemental impurities in drug products may arise from several sources; they may be residual catalysts that were added intentionally in synthesis or may be present as impurities ( , through interactions with processing equipment or container/closure systems or by being present in components of the drug product). Because elemental impurities do not provide any therapeutic benefit to the patient, their levels in the drug product should be controlled within acceptable limits. There are three parts of this GUIDELINE : the evaluation of the toxicity data for potential elemental impurities ; the establishment of a Permitted Daily Exposure (PDE) for each element of toxicological concern; and application of a risk- based approach to control elemental impurities in drug products.

8 An applicant is not expected to tighten the limits based on process capability, provided that the elemental impurities in drug products do not exceed the PDEs. The PDEs established in this GUIDELINE are considered to be protective of public health for all patient populations. In some cases, lower levels of elemental impurities may be warranted when levels below toxicity thresholds have been shown to have an impact on other quality attributes of the drug product ( , element catalyzed degradation of drug substances). In addition, for elements with high PDEs, other limits may have to be considered from a pharmaceutical quality perspective and other guidelines should be consulted ( , ICH Q3A).

9 This GUIDELINE presents a process to assess and control elemental impurities in the drug product using the principles of risk management as described in ICH Q9. This process provides a platform for developing a risk-based control strategy to limit elemental impurities in the drug product. 2. SCOPE. The GUIDELINE applies to new finished drug products (as defined in ICH Q6A and Q6B) and new drug products containing existing drug substances. The drug products containing purified proteins and polypeptides (including proteins and polypeptides produced from recombinant or non-recombinant origins), their derivatives, and products of which they are components ( , conjugates) are within the scope of this GUIDELINE , as are drug products containing synthetically produced polypeptides, polynucleotides, and oligosaccharides.

10 This GUIDELINE does not apply to herbal products, radiopharmaceuticals, vaccines, cell metabolites, DNA products, allergenic extracts, cells, whole blood, cellular blood components or blood derivatives including plasma and plasma derivatives, dialysate solutions not intended for systemic circulation, and elements that are intentionally included in the drug product for therapeutic benefit. This GUIDELINE does not apply to products based on genes (gene therapy), cells (cell therapy) and tissue (tissue engineering). In some regions, these products are known as advanced therapy medicinal products. This GUIDELINE does not apply to drug products used during clinical research stages of development.