Transcription of ACTIVE PHARMACEUTICAL INGREDIENTS …
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ACTIVE PHARMACEUTICAL INGREDIENTS COMMITTEE (APIC). eCTD HOW TO DO DOCUMENT. July 2014. APIC_eCTD How to Do Table of Content 1. CHAPTER 1: REGULATORY FRAMEWORK & NATIONAL Introduction: view of authorities in general & trend ..5. Requirements for the European Union ..5. Requirements for EU Countries ..6. European Medicines Agency (EMA) ..7. Requirements for the United States of America ..7. Requirements for Japan ..8. Requirements for 2. CHAPTER 2: OPTIONS & CONSIDERATIONS FOR API MANUFACTURERS TO. HANDLE E-CTD REQUIREMENTS ..9. Evaluation of current submission processes & tools ..9. Boundaries ..10. User Requirement Specification (URS).
APIC_eCTD How to Do Page 6 Requirements for electronic files Electronic files should be in accordance with the Guidance for Industry on Providing Regulatory
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