Overview

This course will provide a full introduction to PIPs and the EU Paediatric Regulation. The course faculty are European-based leading experts from EMA and industry. Topics will be presented through interactive lectures and hands-on workshop training.

What you will learn

EU paediatric regulation
PIP lifecycle
How to get your PIP approved
PIPs after approval

Who should attend?

Professionals in regulatory affairs, clinical research, project management, toxicology, product development.

Participants should preferably have a fair understanding of aspects of paediatric medicines development.

Level: Intermediate

Learning objectives

At the conclusion of this course, participants will be able to:

Describe the EU paediatric regulation
Discuss the PIP approval procedure
Identify the expectations and requirements from the Paediatric Committee (PDCO)
Demonstrate how to prepare a PIP eligible for evaluation by PDCO
Explain the modification of an agreed PIP procedure
Describe the compliance check procedure
Demonstrate an overview of procedures after initial PIP approval

Participants will complete a knowledge check at the end of the course and will be provided with feedback to ensure learning objectives are attained.

Plan Your Team's Professional Development

Why not take advantage and train your whole department (or even across different departments!) and benefit from increased:

Focus
Flexibility
Convenience
Cost Effectiveness

For more information please contact EMEA@DIAglobal.org

Digital Learning Catalog

Download

Have an account?

Register

Paediatric Investigation Plans (PIP)