EMA paediatric investigation plans in-person training course
Learn about paediatric investigation plans (PIPs) directly from regulators and industry experts.
EventHumanPaediatrics
French is available via eTranslation, the European Commission's machine translation service.
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- The original event times are:
- Jeudi, novembre 5, 2026 - 08:00 - 18:00 Amsterdam time (CET)
- Vendredi, novembre 6, 2026 - 08:30 - 16:30 Amsterdam time (CET)
Date
- , -, -
Emplacement
- European Medicines Agency, Amsterdam, the Netherlands
Event summary
Gain a practical understanding of the EU Paediatric Regulation and Paediatric Investigation Plans (PIPs). This hands-on course supports professionals involved in paediatric medicine development and regulatory submissions.
Why attend
Learn how to navigate paediatric regulatory requirements and prepare high-quality submissions with confidence.
How you learn
Experts from the European Medicines Agency and industry lead the course through:
- Interactive lectures
- Real-world case discussions
- Practical workshop sessions
- Direct engagement with regulators and experienced professionals
Course outcomes
By the end of the course, participants can:
- Understand the EU paediatric regulatory framework
- Apply key principles of Paediatric Investigation Plans (PIPs)
- Address regulatory requirements effectively
- Prepare comprehensive paediatric submissions
- Strengthen expertise in paediatric drug development
This course provides a strong foundation for both newcomers and experienced professionals seeking to expand their knowledge of paediatric regulation.
Registration
Registration is open via the below link: