The trainer is very clear, the course is very interesting and easy to follow. She provides very good examples. I liked how the full course is presented from a CRO perspective which makes it very useful for its application on clinical trial activities. It is very useful that it is focusing on the application of the

The training was very well designed and presented. The information given, was appropriate and very detailed - easy to follow and understand.

I got a solid idea in which who is responsible of what when conducting a clinical research considering regulatory elements both national and EU legislation of the clinical trials. I liked the motto 'Think European, act national' when considering starting to work as a CRA, having this motto in the pocket to ensure patients safety and

The training has given me not only basic knowledge regarding guidelines and regulations necessary in Clinical Trial life cycle but also where to find them in case I need them. That is, the training provided enough materials and links online to deepen one's knowledge in regards with European and International guidelines and legislation in CT. The

I have certainly gained a deeper understanding of the main regulations required at various stages of a clinical trial. Thanks to this course, I have learned how crucial it is to pay attention to the documents required for the proper conduct of a trial. I will focus on studying the most important laws, regulations, and declarations,

Through the "Basics of Regulatory Requirements in Clinical Research" course at ECCRT, I have achieved the following objectives: 1. Knowledge: Gained a comprehensive understanding of regulatory frameworks and requirements in clinical research. 2. Skills: Developed the ability to apply regulatory guidelines to ensure compliance in clinical trials. 3. Behavior: Enhanced my attention to detail and adherence

The course provided me with answers regarding the flow of work regarding obtaining the approval in EU. What type of clinical trials require what kind of documents. Another important point that I noted for myself is clear role and responsibility of stakeholders on different approval of documents such as the adverse events reporting, annual reports, archive

I've acquired new knowledge regarding regulatory requirements and, most importantly, I've learned how rigorous their application must be to protect the subjects involved in clinical trials and ensure the quality and reliability of the results obtained. I will adhere strictly to ethical and legal guidelines, ensuring compliance in all aspects of clinical research. The material is

Great overall experience: the content of the course was on point, the duration of the videos were adequate, and the teacher was really engaging. The quizzes at the end of some of the chapters were very helpful to test the acquired knowledge!

It is a great opportunity to improve your knowledge about clinical studies and get also an official evidence of completion for any future career possibilities.