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 […]
Get an introduction to the Ethical Rules for the Pharmaceutical Industry in Sweden (LER) via this e-course. You will be aware of the most important rules and guidelines that regulate […]
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 […]
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 […]
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 […]
Join us in exploring cutting-edge computational chemistry, including topics such as Machine Learning and Artificial Intelligence, Structure- and Ligand-based drug design, and the Design of Nucleotides, Peptides, and Proteins. […]
This course is aimed at those with regulatory experience in pharmaceuticals who wish to deepen their knowledge of the medical device aspects of combination products (drug-device). It consists of an […]
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 […]
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 research […]
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 […]