Explore Module 1 free of charge, no registration required. Register later to access the first test and the remaining four modules, or register now for immediate access to the complete five-module training.
\r\nAccess the first module for free here
\r\nThis online training covers the ethical, regulatory, and operational aspects of clinical research. Participants will learn the principles of ICH GCP (R3) and ISO 14155:2026, as well as the requirements of key European regulations and Polish national legislation governing medicinal product, medical device, and in vitro diagnostic studies.
\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\nThe course consists of five modules, each lasting approx. 60 minutes:
\r\n\r\nThe modules must be completed in the specified order. The tests each contain 10 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. The narration in this course uses an AI-generated synthetic voice. All educational content has been reviewed and approved by qualified human experts.
\r\n\r\n\r\n\r\nThis flexible training allows participants to learn at their own pace, ensuring accessibility for busy professionals. Upon successful completion of all modules and assessments, participants in the full course receive a downloadable GCP Certificate.