All of the topics were presented with excellence by a very competent and very experienced trainer. It was a combination of key auditing information and practical tips on application. The attendees of 5 clinical research professionals with various positions and backgrounds made theinteractive discussions and the inputs very interesting and multi-facetted. I also appreciate the helpful

The trainer is clearly an expert in the field, and is a clear and calm presenter, who gave good explanations and examples. It was not an easy topic, but the course was well and thoroughly prepared.  In the future I will read contracts with more knowledge and in a different light.

I have worked in clinical research for nine years, not on vaccines. I am about to start a new job working in vaccine development, so I did the ECCRT course to obtain a quick overview of vaccine development and to highlight areas of similarity and difference from my experience in drug development. The course was excellent

The course was very good - well organised and sufficient time for discussion and  questions.

SUPER trainer, who gives good explanation, provides a lot of examples and tips and who is sharing expertise.

The trainer gave a very good presentation and the materials were on the spot.The course was interactive and targeted at the audience's needs.

The theory and debate around informed consent was a very important issue.  We had a very nice discussion and received good suggestions.

The course gave me an excellent overview of Safety and Serious Adverse Events (SAE) procedures.

Surprisingly I learned a lot in this short time. The course was very interactive and never boring. I would recommend the course to my colleagues even if they are not CRAs.

2 years after our tailored GCP-training we came back to ECCRT for a ICH-GCP refresher course.  We would like to thank you again, the course was well organized and very captivating and interesting.  We are back up to date and our acute questions are resolved.