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 […]
The symposium in honour of Professor Pieter Cullis work promises to be a stimulating and informative event that highlights the remarkable achievements of one of the leading figures in groundbreaking […]
Are you looking for broad and essential knowledge of Regulatory Affairs? Our popular 3-day course in fundamental Regulatory Affairs gives a comprehensive picture and is a platform for your further […]
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 […]
