OVERVIEW

Clinical Research in Pediatric Oncology is organized by Princess Maxima Center / Prinses Maxima Centrum and will be held from Jul 01 - 04, 2025 at Hotel & Conference Centre Landgoed Zonheuvel, Doorn, Utrecht, Netherlands.

Description:
How do I design and write a clinical trial or treatment protocol? A highly interactive theoretical and practical workshop.

Are you eager to learn how to write a late phase clinical drug trial or treatment protocol? Meet our international faculty who will teach you the tricks of the trade and provide expert input on your draft synopsis.

This 4-day workshop aims to train early-career clinicians who want to get involved in clinical research to design and write a study synopsis for a late phase clinical drug trial or a treatment protocol within the context of (mainly) European legislation. The workshop is endorsed by SIOP.

This highly interactive theoretical and practical 4-day workshop aims to train early-career clinicians who want to get involved in clinical research in pediatric oncology  to write a synopsis for a high quality late phase clinical drug trial or a treatment protocol for children with cancer, in the context (mainly) of European legislation.  This comprehensive synopsis can be used as a basis to finalize and implement a study or treatment protocol in the participant’s local setting.

Exclusive Hands-On Workshop
The workshop consists of 4 Live Days preceded by an extensive online program.  

During the pre-program, you will get an extensive overview of the overall context of all key aspects of clinical drug research in children with cancer. You can use this pre-program to prepare for the Live Days.

During the first 3 Live Days, you will be trained further in the theoretical aspects of designing and writing a study synopsis for a late phase clinical trial or treatment protocol. Interactive lectures given by highly experienced (inter)national faculty members will provide you with an overview of the building blocks of designing and implementing high quality clinical trials. During focus sessions and expert panels, specific issues raised during these sessions will be discussed in greater depth.

In the afternoon, you will follow hands-on workshops and will have dedicated time to work on your synopsis using the knowledge acquired in the morning. Faculty members will coach you to improve your synopsis during small group discussions and one-to-one sessions.

During the 4th day, you will complete the synopsis or summary and present it to your peers.

KEY DATES

Event Start Date
01 Jul, 2025
Event Start Date
Event End Date
04 Jul, 2025
Event End Date
Credits

CME Accreditation
The application for Accreditation will be submitted to the European Accreditation Council for CME (EACCME) of the European Union of Medical Specialists (UEMS).

The workshop has been awarded by the European Accreditation Council for Continuing Medical Education (EACCME®) for a maximum of 27.0 European CME credits (ECMEC®s) for live participation and about 10.0 CME credits for online participation. 

  • 27 ECMECs
  • TARGET AUDIENCE

    PhysicianCliniciansOncologistsClinical ResearchersPediatrics

    SPECIALITIES

    Pediatric OncologyResearch and Clinical Research

    SUGGESTED HOTELS

    CONFERENCE VENUE

    LocationHotel & Conference Centre Landgoed Zonheuvel
    Amersfoortseweg 98

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