Klinische studies voor professionals

Below are the steps that must be followed before a study can start.

1. Registering the study:

The sponsor of a clinical trial should first registers the study by means of the registration form. After that, you will receive an email from the relevant study nurse or study coordinator with more information about the next steps.

2. Contracts

Some guidelines for drawing up a study contract with our hospital can be found here.

3. Ethics Committee

Chairman: Mr Johan Vandenbulcke

Contact: Ms Chantal Catteeuw

• Function: secretary of the Ethics Committee
• Email: chantal.catteeuw@yperman.net
• T +32 57 35 70 43
• F +32 57 35 36 37

Hospital approval number: 057

Accreditation number: 71005780 000

Please mail all documents to chantal.catteeuw@yperman.net
Please cc studies@yperman.net.

4. Contact

If you would like more information on the preparation and the course of clinical studies, feel free to contact the study coordinator: Ria Vandenbrande
Student nurses: Florence Havegheer or Marijke Ghekiere

Accessibility: Jan Yperman Ziekenhuis, Briekestraat 12, 8900 Ieper, route 98