I have learned a lot of practical tips for a CRA. Liesbeth also gave a lot of examples, what makes the theory more accessible. Liesbeth is a very enthusiastic and experienced trainer. It was 2 long intensive days, but this made sure we were fully into the course.

Good group, presentation, and tools to handle problematic situations allowing me to become more assertive in my communication and behaviour.

I understood more about the world of clinical research and the different figures involved in it. I really appreciated the friendly and interactive environment and the curiosity inspired by the trainer

I feel like I have a good overall idea of the everyday work of a CRA. It was good to have some hands-on training for the monitoring activities as well. It was great to see how interactive the course was and how it was possible to ask questions and engage in conversation.

It was a very nice training to cover all basics of the legal parts of a contract including data protection, well done. The training sessions are really well managed and planned. All the different examples during the course were really helpful to understand the topics best.

A structured approach to managing clinical studies, the course templates will also be useful to help implement this. Thanks to this training, I gained more knowledge around clinical research and project management.

Good overview of the process, and good tips to follow when contracting a CRO. It can be useful for the management of CROs.

Regular quiz and workshops, good documentation, presentation well structured. Very good interactivity to keep your focus on the subject and avoid 'weariness'.

A good way of learning with the quizzes and the workshop during the course. It is refreshing knowledge of GCP and ensures the tasks are done correctly at my company.

The training was very organized with good material, topics, and exercises. I recommend this course because it gives more information about Clinical Trials. All things needed for a Clinical Trial are in this course (from the collection of data till the end of the Trial).