I learned about the monitoring activities at different stages of a clinical trial, from study subject recruitment to safety reporting and quality assurance. Additionally, I gained an understanding of the applicable legislation, ensuring compliance throughout the trial process. I will apply the knowledge of monitoring activities at different stages of a clinical trial. It was nice

I got familiar with positions available within clinical research and it was of particular importance for start-up people, enabling the narrowing of future job applications for more suitable positions according to individual characteristics. The engaging and multidimensional structure of the course was followed by the positivity and encouragement of the tutor ,it was a nice open conversation with

Good refresher for the course I took 10+ years ago. Update on regulations and inspector expectations. Practical tips in outsourcing setting - The exercise and possibility to ask questions related to actual operational challenges at own company.

This course gives you a complete overview on different roles in the clinical research.

It was a very personalized course where you can openly make questions and clarify doubts, also the great experience of the instructor in the clinical research area, helps you to understand everything in a simple clear way!

ECCRT is very helpful and the information given during the training can easily solve anyone's doubts about career path!

Very interactive webinair with some practical workshop, tips and tools!

small diverse group with great interaction and a good overview of tasks of an advanced project manager!

The course was very interactive. I liked having the opportunity to ask questions and get desirable answers.

I learned very detailed the procedures for running medical device trials (project coordination, content, regulations, practical doing etc.); ISO, GCP - intensive discussions, benefit from the extensive experience of the trainer; extensively pleasant atmosphere.