/ Continuing Education
NEW: Safety Management in Clinical Research
Free-of-charge online courses on the definitions, requirements and procedures related to safety management in clinical research.
Topics:
- Legal and regulatory framework of safety reporting
- Assessment of adverse events
- Documentation and reporting of adverse events
- Safety and protective measures
- Annual Safety Reports
Different types of studies defined by the Human Research Act (HRA) are covered in two different courses:
Course 1: Safety Management in Clinical Research
- Clinical trials with medicinal products
- Other clinical trials
- Human research projects
Course 2: Safety Management in Clinical Research
- Clinical trials with medical devices