Guideline published on: 24/09/2026
Good Manufacturing Practice (GMP) provides the foundation for ensuring that medicinal products are consistently manufactured and controlled according to appropriate quality standards.
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- The Use of Data in Public Health. Understanding the Potential for Artificial Intelligence in Medicine
- UK Government confirms indefinite recognition of CE marked medical devices
- Methodological Principles for the Assessment of Section 5.1 of the Summary of Product Characteristics
- Good manufacturing practice (GMP) Multistakeholder workshop on expert contributions to artificial intelligence guidance development (Annex 22)
- PIC/S PE 009-18 – Guide to GMP for Medicinal Products | Part I
- EMA Updates Information Page on Bioequivalence Guidelines
- FDA Issues Guidance on Identity and Safety Information for New Dietary Ingredient Notifications
- Data Quality Framework for EU Medicines Regulation: Application to the Collection, Management and Submission of Adverse Drug Reaction Reports