This e-course provides a solid introduction to the key steps involved in bringing a medical device to market. It covers the essentials of the development process, incorporating interactive elements and […]
This e-course invites you to explore the Life Science landscape with an overview of key players, regulations, product categories, and Swedish Life Science organizations. Gain insights into job functions within […]
Do you want to know how to access the Nordic Nordic pharmaceutical market? To succeed, you need to be familiar with similarities and differences between the countries. In this e-course, […]
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 requirements have become even more stringent. This course provides an overview of the regulatory requirements for drug-device combination products, with a specific emphasis on the […]
Build your Regulatory Affairs and life science expertise with Läkemedelsakademin. A program of 11 courses designed for you who aspire to work within regulatory affairs in the pharmaceutical industry. Whether […]
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
Early Bird Fee until March 1 2027.
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 […]
Nordic-Baltic Regulatory Affairs Meeting 2027 brings the Nordic-Baltic authorities and pharmaceutical industry operators together on the latest news about the hottest topics discussed within Regulatory Affairs. Welcome! View full […]