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 knowledge checks to enhance your learning experience. View full course information
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 the companies’ promotion of medicines as well as their interaction with healthcare professionals and the general public. View Full course information
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 the field, along with a glimpse into the latest technologies and innovations. View full course information
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 you are already on your regulatory affairs career path, or you currently work in another area of the life science sector ,the Academy is here […]
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, you learn about stakeholders, regulations and processes. View full course information
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 […]
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 drug delivery systems and offers an opportunity for researchers to engage in meaningful discussions and collaborations. Drug delivery of new drug modalities using lipid nanoparticles […]
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 development in the area. View full course information
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 leading Swedish scientists. The meeting provides an excellent forum for networking with colleagues active in the field. To conference 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
