Learn the essential requirements for ensuring that medical devices meet usability standards in Europe and the United States. This course provides insights on how to practically apply the regulations to ensure compliance and successfully launch your product on the market. View full course information
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 sneak-peak into the near future solutions. View full course information
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 research or marketing company. View full course information
Medicon Village, Lund
Scheelevägen 1, Lund, Sverige
This symposium aims to explore current challenges in the field of solid oral dosage forms, with focus on both theoretical and manufacturing perspectives. It will cover a broad range of topics relevant to both industry and academia, including advancements in modeling and digital tools, innovations in manufacturing processes and excipients, sustainability practices, life cycle analysis, […]
The development of biologic 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 key aspects of biologic development, from discovery to launch. View full course information
Nordic Regulatory Affairs Meeting 2025 brings the Nordic authorities and pharmaceutical industry operators together on the latest news about the hottest topics discussed within Regulatory Affairs. Welcome! View full course information
Kakor
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