Regulation (EU) 2024/568: Questions and answers clinic for the Human Industry stakeholders
EventHumanFees
On Monday, 12 January 2026, between 07:00 and 10:00 CET (Amsterdam time), this website will be unavailable due to scheduled maintenance.
- The original event time is:
- Monday, February 10, 2025 - 11:00 - 12:00 Amsterdam time (CET)
Date
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Location
- OnlineEuropean Medicines Agency, Amsterdam, the Netherlands
Event summary
On 1 January 2025, Regulation (EU) 2024/568 on fees and charges payable to the European Medicines Agency ('New Fee Regulation' (“NFR”)) came into force.
The Agency invites all human industry stakeholders to a questions and answers session on the regulatory and system changes resulting from the introduction of this regulation (e.g., the introduction of the new Certificates processing System or CPS).
Ahead of the session, we encourage you to consult the following materials:
- Regulation (EU) 2024/568
- Questions and answers on NFR
- Fee Regulation Working Arrangements
- Guidance on how to pay fees to EMA
- Guidance on how to request Certificates via the new CPS
Please note: technical questions related to any other system changes or platforms (e.g., IRIS) except for CPS are outside the scope of this session.
Registration
- To attend the session, please register here.
- Participants are encouraged to submit questions in advance