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 enable marketing within Europe. 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
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 key aspects of development, from discovery to launch. Course information
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 future growth in the field.
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 to the inspection process and common findings, to be able to prepare for and conduct inspections successfully. Course information
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 area. View full course information