The course includes five key modules. This structured training ensures participants gain the necessary knowledge to conduct clinical research ethically and in compliance with Polish and international standards.

Clinical Trials and Regulations in Poland and ISO14155

The course covers the fundamentals of the Declaration of Helsinki and ISO14155, explains the roles and responsibilities of investigators and sponsors, presents current laws and guidelines, and provides a practical overview of medical device studies, ensuring participants gain essential knowledge for conducting clinical trials in compliance with Polish and international regulations.

After completing all modules, the Premium version gives you a certificate which you can download conveniently online. It also gives you access to training materials to 2 months, which can be further extended upon request.

The modules must be completed in the specified order. Each module consists of a 45-60 minute presentation followed by a test to assess learning progress.

The tests each contain 15 randomized questions from a question bank. Participants have three attempts per test, with randomized questions for each attempt. A minimum of 80% correct answers is required to proceed with the course. Answering the test questions takes approximately 15 minutes.

This flexible training allows participants to learn at their own pace, ensuring accessibility for busy professionals.