ICH HARMONISED TRIPARTITE GUIDELINE

1 INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL. REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE. ICH HARMONISED TRIPARTITE GUIDELINE . GOOD MANUFACTURING PRACTICE GUIDE FOR. active pharmaceutical ingredients . Q7. Current Step 4 version dated 10 November 2000. 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, Japan and USA. Q7. Document History New First Codification History Date Codification November 2005. Q7A Approval by the Steering Committee under Step 2 and 19 Q7.

2 Release for public consultation. July 2000. Current Step 4 version Q7A Approval by the Steering Committee under Step 4 and 10 Q7. recommendation for adoption to the three ICH regulatory November bodies. 2000. GOOD MANUFACTURING PRACTICE GUIDE FOR. active pharmaceutical ingredients . ICH HARMONISED TRIPARTITE GUIDELINE Having reached Step 4 of the ICH Process at the ICH Steering Committee meeting on 10 November 2000, this GUIDELINE is recommended for adoption to the three regulatory parties to ICH. TABLE OF CONTENTS. 1. 1. Objective .. 1. Regulatory Applicability .. 1. Scope .. 1. 2. QUALITY MANAGEMENT .. 4. Principles .. 4. Responsibilities of the Quality Unit(s).. 4. Responsibility for Production 5.

3 Internal Audits (Self Inspection).. 5. Product Quality Review .. 6. 3. PERSONNEL .. 6. Personnel 6. Personnel Hygiene .. 6. 7. 4. BUILDINGS AND 7. Design and Construction .. 7. Utilities .. 8. Water .. 8. 8. Lighting .. 9. Sewage and 9. Sanitation and Maintenance .. 9. 5. PROCESS 9. Design and Construction .. 9. Equipment Maintenance and Cleaning .. 10. 11. Computerized 11. i Good Manufacturing Practice Guide for active pharmaceutical ingredients 6. DOCUMENTATION AND RECORDS ..12. Documentation System and Specifications ..12. Equipment Cleaning and Use Records of Raw Materials, Intermediates, API Labelling and Packaging Materials ..13. Master Production Instructions (Master Production and Control Records).

4 13. Batch Production Records (Batch Production and Control Records) ..14. Laboratory Control Records ..14. Batch Production Record Review ..15. 7. MATERIALS General Controls ..16. Receipt and Quarantine ..16. Sampling and Testing of Incoming Production Materials ..16. Re-evaluation ..17. 8. PRODUCTION AND IN-PROCESS CONTROLS ..18. Production Time Limits ..18. In-process Sampling and Controls ..18. Blending Batches of Intermediates or APIs ..19. Contamination Control ..20. 9. PACKAGING AND IDENTIFICATION LABELLING OF APIS AND. INTERMEDIATES ..20. General ..20. Packaging Materials ..20. Label Issuance and Packaging and Labelling 10. STORAGE AND DISTRIBUTION ..22. Warehousing Procedures ..22. Distribution Procedures.

5 22. 11. LABORATORY CONTROLS ..22. General Controls ..22. Testing of Intermediates and APIs ..23. Validation of Analytical Procedures - see Section Certificates of Stability Monitoring of APIs ..24. Expiry and Retest ii Good Manufacturing Practice Guide for active pharmaceutical ingredients Reserve/Retention Samples .. 25. 12. VALIDATION .. 25. Validation Policy .. 25. Validation 26. Qualification .. 26. Approaches to Process Validation .. 26. Process Validation Program .. 27. Periodic Review of Validated Systems .. 27. Cleaning Validation .. 28. Validation of Analytical Methods .. 28. 13. CHANGE CONTROL .. 29. 14. REJECTION AND RE-USE OF 29. Rejection .. 29. Reprocessing .. 29. 30. Recovery of Materials and Solvents.

6 30. Returns .. 31. 15. COMPLAINTS AND RECALLS .. 31. 16. CONTRACT MANUFACTURERS (INCLUDING LABORATORIES) .. 31. 17. AGENTS, BROKERS, TRADERS, DISTRIBUTORS, REPACKERS, AND. 32. Applicability .. 32. Traceability of Distributed APIs and 32. Quality Management .. 33. Repackaging, Relabelling and Holding of APIs and Intermediates .. 33. Stability .. 33. Transfer of Information .. 33. Handling of Complaints and 33. Handling of 34. 18. SPECIFIC GUIDANCE FOR APIS MANUFACTURED BY CELL. CULTURE/FERMENTATION .. 34. General .. 34. Cell Bank Maintenance and Record Keeping .. 35. Cell Culture/Fermentation .. 35. Harvesting, Isolation and 36. Viral Removal/Inactivation steps .. 36. iii Good Manufacturing Practice Guide for active pharmaceutical ingredients 19.

7 APIS FOR USE IN CLINICAL TRIALS ..37. General ..37. Equipment and Facilities ..37. Control of Raw Materials ..37. Production ..38. Validation ..38. Changes ..38. Laboratory Documentation ..38. 20. iv GOOD MANUFACTURING PRACTICE GUIDE FOR. active pharmaceutical ingredients . 1. INTRODUCTION. Objective This document (Guide) is intended to provide guidance regarding good manufacturing practice (GMP) for the manufacturing of active pharmaceutical ingredients (APIs) under an appropriate system for managing quality. It is also intended to help ensure that APIs meet the requirements for quality and purity that they purport or are represented to possess. In this Guide manufacturing is defined to include all operations of receipt of materials, production, packaging, repackaging, labelling, relabelling, quality control, release, storage and distribution of APIs and the related controls.

8 In this Guide the term should . indicates recommendations that are expected to apply unless shown to be inapplicable or replaced by an alternative demonstrated to provide at least an equivalent level of quality assurance. For the purposes of this Guide, the terms current good manufacturing practices and good manufacturing practices are equivalent. The Guide as a whole does not cover safety aspects for the personnel engaged in the manufacture, nor aspects of protection of the environment. These controls are inherent responsibilities of the manufacturer and are governed by national laws. This Guide is not intended to define registration/filing requirements or modify pharmacopoeial requirements. This Guide does not affect the ability of the responsible regulatory agency to establish specific registration/filing requirements regarding APIs within the context of marketing/manufacturing authorizations or drug applications.

9 All commitments in registration/filing documents must be met. Regulatory Applicability Within the world community, materials may vary as to the legal classification as an API. When a material is classified as an API in the region or country in which it is manufactured or used in a drug product, it should be manufactured according to this Guide. Scope This Guide applies to the manufacture of APIs for use in human drug (medicinal) products. It applies to the manufacture of sterile APIs only up to the point immediately prior to the APIs being rendered sterile. The sterilization and aseptic processing of sterile APIs are not covered by this guidance, but should be performed in accordance with GMP guidelines for drug (medicinal) products as defined by local authorities.

10 This Guide covers APIs that are manufactured by chemical synthesis, extraction, cell culture/fermentation, by recovery from natural sources, or by any combination of these processes. Specific guidance for APIs manufactured by cell culture/fermentation is described in Section 18. This Guide excludes all vaccines, whole cells, whole blood and plasma, blood and plasma derivatives (plasma fractionation), and gene therapy APIs. However, it does include APIs that are produced using blood or plasma as raw materials. Note that cell substrates (mammalian, plant, insect or microbial cells, tissue or animal sources including transgenic 1. Good Manufacturing Practice Guide for active pharmaceutical ingredients animals) and early process steps may be subject to GMP but are not covered by this Guide.