e/MTIC 'Clinical Regulatory'


The e/MTIC courses are organized for e/MTIC researchers. These courses are also open to participants from other TU/e health care related projects (from TU/e and external partners). If  not directly e/MTIC related and interested in joining the e/MTIC courses, please send your question on participation to smpee@tue.nl

Similar Course - Philips
If you have already taken a similar course in the past within Philips (like Introduction to ICBE Processes for Research, Introduction to Regulations for Research, Good Documentation Practices for Medical Device Manufacturers etc.) then you already have the required knowledge and you do not need to enroll again.

Course contents

We will discuss the fundamentals of Good Clinical Practice (GCP) and the Dutch regulatory framework including the role and the responsibilities of the researchers involved.

Furthermore, the process workflow within e/MTIC studies and the respective institutes and where to find support documentation (templates) will be highlighted.

Course objective

After the course, you will have an understanding of the regulatory framework and basic knowledge of the first steps to set-up a clinical trial. In addition, you will know where to find the necessary required information and support within TU/e and e/MTIC related institutions.

Course information

2023 - A new date will be communicated A.S.A.P.

  • Date: not yet known
  • Time: 14-17 hrs
  • Location: TU/e, room not yet known
  • Presented by Susan Hommerson
  • Costs: free of charge. With a No Show, we will need to charge you € 50.
  • You can cancel upto Monday, date not yet known, 12:00 hours.
  • This course is obligatory for all e/MTIC PhD’s and PostDocs.
  • To register, click here. Registration is not possible now

Course coordination