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 conference is sold out, if you would like to sign up for the waiting list, please send an email to jenny.hagberg@lakemedelsakademin.se View full conference information
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 ensure compliance and successfully launch your product on the market. 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
This symposium aims to explore current challenges in the field of solid oral dosage forms, with focus on both theoretical and manufacturing perspectives. It will cover a broad range of topics relevant to both industry and academia, including advancements in modeling and digital tools, innovations in manufacturing processes and excipients, sustainability practices, life cycle analysis, […]
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 all key aspects of biologic development, from discovery to launch. View full course information