Join our interactive Webinar as we introduce and discuss the publication of the tenth edition of WHO Good Manufacturing Practices (GMP) Compendium and related guidelines. This session is ideal for healthcare professionals, regulatory affairs specialists, quality assurance professionals, pharmaceutical manufacturers, GMP inspectors, and all stakeholders dedicated to ensuring the quality, safety and efficacy of pharmaceutical products.
We will:
- Get an in-depth look at the latest edition's update covering a total of forty-six guidelines on GMP and inspection-related topics;
- Present the newly introduced guidelines, such as GMP for investigational radiopharmaceuticals, medicinal gases, and more;
- Present the revised guidelines that incorporate recent advancements and address emerging challenges in the pharmaceutical industry;
- Discover how the Compendium simplifies access to and implementation of WHO's guidelines.
In this Webinar, you will learn:
- About the current and most updated WHO guidelines and related materials on GMP and inspection-related topics;
- How to navigate and utilize the Compendium and the guidelines repository with ease.
Whether involved in manufacturing, regulatory compliance, or quality control, this webinar will provide you with valuable insights into a tool that aids countries in establishing robust regulatory systems and upholding international standards in pharmaceutical quality assurance.