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The DCR demonstrated a rapid and effective response to the 2025 revisions of the Swiss Human Research Act (HRA) ordinances by promptly updating its courses and training materials to reflect the latest regulatory requirements. As new transparency measures, informed consent procedures, and data governance expectations came into effect, the DCR ensured that all relevant educational content remained fully aligned with current national standards for human research.

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Course Updates & Exclusive GCP Refresher Course for Inselspital Staff

Course curricula were reviewed and revised in close collaboration with subject matter experts to incorporate the updated HRA guidance, including changes related to clinical trial registration, reporting obligations, e-consent, and the handling of health-related data and biological materials. Through timely updates to courses, workshops, and supporting resources, participants received practical and up-to-date instruction on the evolving ethical and legal framework governing research in Switzerland. Particular effort was made to update Inselspital Clinical Research Staff with two special GCP Refresher course, which was visited by 355 participants.

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By responding quickly to these ordinance changes, the DCR reinforced its commitment to providing current, high-quality research education. This proactive approach ensures that researchers, students, and clinical staff are equipped with the latest knowledge and competencies required for compliant and ethically responsible research practices.


Find all DCR courses here.

What is the HRA?

The Human Research Act (HRA) is the Swiss federal law that regulates research involving human participants, health-related data, and biological material to promote ethical standards, participant protection, and scientific integrity.

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