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Explore EU regulatory affairs
Courses at this level are for:
People wanting to take their first steps in regulatory affairs
People in other disciplines who need an overview
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09/03/2027
Essentials of European Veterinary Regulatory Affairs
The world of veterinary regulatory affairs can be a confusing and complex place, particularly if you have no formal veterinary or regulatory affairs background. The purpose of this course is to provide you with a clear and concise understanding of the role played by regulatory affairs in obtaining and maintaining marketing authorisations for veterinary medicinal products.
VETB0227O
06/04/2027
Essentials of European Medical Device Regulatory Affairs
Gain a practical introduction to European medical device regulations and the regulatory affairs profession. Explore key requirements including CE marking, device classification, conformity assessment and post-market surveillance, enabling you to support compliance with confidence.
BASMD0527O
05/05/2027
Essentials of European Pharmaceutical Regulatory Affairs
Build a strong foundation in European pharmaceutical regulatory affairs and gain the knowledge needed to start or advance your career in the profession. Explore the regulatory framework for medicines, marketing authorisations, product lifecycle management and key regulatory procedures, enabling you to contribute with greater confidence and effectiveness.
BAS0427O
13/07/2027
Essentials of In Vitro Diagnostics Regulatory Affairs
Build a strong foundation in in vitro diagnostics (IVD) regulatory affairs and gain the knowledge needed to work confidently within this evolving sector. Explore key regulatory requirements, product performance principles, documentation and approval processes, enabling you to support compliance and contribute effectively across the IVD product lifecycle.
BASIVD27O
05/10/2027
Essentials of European Pharmaceutical Regulatory Affairs
Build a strong foundation in European pharmaceutical regulatory affairs and gain the knowledge needed to start or advance your career in the profession. Explore the regulatory framework for medicines, marketing authorisations, product lifecycle management and key regulatory procedures, enabling you to contribute with greater confidence and effectiveness.
BAS1027O
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