The course provides an overview of the regulations governing medical devices and how to apply them in practice. You’ll gain insight into the requirements for both manufacturers and products to […]
Join us to hear from speakers with experience in contracting and working with CDMOs and gain valuable insights into best practices and strategies.
Join a key Nordic meeting point for everyone involved in clinical trials. Two days of insight, exchange and valuable networking await. View full conference information
This conference targets academic and industrial scientists engaged in all aspects of drug discovery and drug development. It aims to showcase the most recent trends in Drug Discovery presented by […]
Get the support you need to ensure regulatory documentation compliance internally and towards authority. This course gives insights and practical advise to current requirements and tools as well as a […]
This two day course gives you the opportunity and tools to be able to contribute strategically to the company in your regulatory role – whether that is at a […]
The development of drugs is a complex, multidisciplinary process involving disease knowledge, target identification, safety principles, and strategies for toxicology, clinical studies, manufacturing, and controls. This three-day course covers all […]
Medical safety is extremely important throughout the life cycle of a drug. The Nordic-Baltic Conference in Pharmacovigilance brings together professionals who have an interest in pharmacovigilance and drug safety to […]
