Back to All Events

Medical Packaging Requirements in the EU and the US


Designed to provide you with an overview of the main requirements and regulations of medical packaging in the EU and the US, this course will help you fully understand the standards of compliance and master the application of the main principles. Join us for this self-paced e-learning course.

Learning Outcomes

At the end of the course, participants will be able to:

  • Understand the principles of medical packaging regulations

  • Analyse the requirements based on the determining factors of administration route and dosage forms

  • Identify the testing requirements and the relevant standards

  • Locate the appropriate competent authority and the contact route if required

Who Should Attend this Course

This course will be most relevant to:

  • Manufacturers and importers of pharmaceutical products and medical devices

  • Manufacturers of packaging materials for pharmaceutical companies

Price

€395,00

Previous
Previous
May 24

Global Monitoring for Sustainability

Next
Next
June 9

Introduction to Life Cycle Assessment