Testimonial Archive - Page 9 of 43 - ECCRT
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I have obtained more knowledge about changes with the new revision R3 of the ICH GCP E6 guideline. I will remember the involvement of all stakeholders is required in the development of study documents such as protocols and ICF's and will inform our clients as such. I personally really liked the table overviews with the cross-check

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.

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!

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