Introduction to this course: 

Discover essential EU GDP guidelines for maintaining medicinal product quality throughout distribution. Explore chapters 1, 2, and 3 of the EU GDP Guideline: quality management, personnel, and equipment requirements. It provides a solid foundation in Good Distribution Practices standards, enhancing your ability to uphold product safety and quality across the supply chain.

Who should attend: 

This course is ideal for anyone involved in distributing, storing, and handling medicinal products, which must ensure compliance with EU GDP guidelines.

Learning Outcomes: 

By the end of this lesson, you will be able to:

• Recall the key components of EU GDP guidelines, including quality management, personnel, and equipment requirements.

• Evaluate potential risks in storage and transportation that could affect medicinal product quality and devise strategies to mitigate them.

What will I gain: 

Participants will gain a thorough understanding of EU GDP compliance. They’ll learn to maintain medicinal product integrity through optimal storage, transportation, and cold chain practices. This knowledge will empower them to ensure regulatory adherence, improve operational efficiency, and uphold the distribution network's highest product safety and quality standards.

Prerequisites: 

Prerequisites for this course include familiarity with pharmaceutical distribution processes and regulatory frameworks.

Additional information: 

Course duration: 00:32:32