Medicinal products intended for use in combination with a medical device is a category that poses additional regulatory challenges. With the implementation of the EU Medical Device Regulation (MDR), the […]
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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
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
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 […]
The symposium aims to connect industry and academic experts working in nasal drug delivery, strengthening collaborations and expanding the national network. It also seeks to engage young scientists to support […]
Are you ready for inspection/audit? This course is designed to give you knowledge and an overview, as well as deeper understanding and experience exchange through discussions on practical issues related […]
Are you looking for broad and essential knowledge of Regulatory Affairs? Our popular 3-day course gives you a comprehensive picture and is a platform for your further development in the […]