{"result": "SUC", "course": 51, "description": "

Maximize Your Clinical Research Career with Our eLearning Modules on Clinical Trials and Regulations in Poland

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

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Clinical Trials and Regulations in Poland: PREMIUM VERSION

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After completing all modules, the Premium version gives you a GCP 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.

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Modules of the Online Training

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The online training consists of five modules, each lasting approx. 60 minutes:

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  1. Development of Drugs and Medical Devices and the Declaration of Helsinki
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  2. Investigator Responsibilities (Part 1)
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  3. Investigator and Sponsor Responsibilities (Part 2)
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  4. Study documents, Ethics Committees and Qualification requirements
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  5. Clinical Trials and Regulations in Poland
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Training Procedure

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The modules must be completed in the specified order. 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.

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Advantages of an online training course

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

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