Module 4: Conclusion – GMP Annex 13 Essentials скачать в хорошем качестве

Module 4: Conclusion – GMP Annex 13 Essentials

Welcome to the concluding module on GMP Annex 13 Essentials. In this video, we’ll recap the key principles of Good Manufacturing Practice for Investigational Medicinal Products, including manufacturing controls, documentation, labeling, distribution, and complaint handling. You’ll see how these elements work together to ensure that every IMP used in a clinical trial is safe, consistent, and compliant with regulatory expectations. We’ll also emphasize how Annex 13 serves as a bridge between GMP and GCP, ensuring quality from production to patient administration. Let’s wrap up by reinforcing how mastering GMP Annex 13 supports both product integrity and trust in clinical research.