Regulatory affairs
Regulatory affairs
Below you will find courses in the category ‘Regulatory Affairs’. These courses focus on topics like: regulation, government affairs and regulating medicines.
- Legislation and Organization for Clinical Researchers (BROK)
- Wet en regelgeving van klinisch-wetenschappelijk onderzoek voor senior onderzoekers
- Global Registration and Approval Process
- European Course for Drug Safety and Pharmacovigilance, ECDS
- Practice of Clinical Trials and Regulation (PFC), Essentials of Clinical Study Management (DIA)
- Drug Regulatory Affairs in Drug Development
- Regulatory Strategic Considerations during Global Drug Development
- Regulatory Affairs in the EU
- Pharmaceutical Policy Analysis Summer School
- Advanced short course in pharmacovigilance
- Intensive Care Research
- Outcomes Assessment, Rational Drug Therapy and Pharmacy
- Pharmacoeconomics: introduction to research methods and applications
