Pre-clinical and early phase are some of the areas that I have the least experience in. This course is very complete and multi-functional and touches upon all aspects involved in moving to FIH. It has been the most interesting course that I have attended in years. Especially the first day was very interesting.

The trainer was able to effectively summarize the quite vast topics addressed in the course. The slides we received could be easily consulted to provide guidance in our day to day work

Ms. Nelle Stocquart executed the course in the excellent interactive manner, using the certain technical tools (like drawing) to keep the audience engaged and really participating in the session. She perfectly followed the core idea of the program - to present the summary of all basic principles and last developments of Clinical trials Regulations in

Real-life examples based on experiences of the trainer as well as doing excercises based on our team issues/behaviors were really appreciated, thanks.   

The interaction, layout of the room and preparation of the trainer resulted in an effective way of learning.   

The greatest aspect of this training was the sharing of experience with others and learning new elements and receiving hints and tips for developing better time management.   

Trainer, workshops and atmosphere really made this learning experience unique.

The many workshops and quizzes in this course made the learning experience great, because they allow a better comprehension of the theory.

This was an excellent course. The quality of the presentations was very high and the trainers were competent, helpful and professional. Questions and interaction were encouraged and this generated useful and informative discussions and made the training interactive and enjoyable as well as informative.   I enjoyed the discussions. I learned a lot from the trainer but also from the experiences of other participants.   

Thorough overview of medical device regulation and great group interaction.