SOP Writing – Workshop
Learn how to improve your SOPs
Get tips and tricks for making your SOPs more practical and easier to understand, so you can ensure greater compliance.
Basic GMP
Understand GMP and learn how companies apply it in practice
This course, which includes evening activities and overnight accommodations, provides you with a solid foundation in GMP.
You’ll learn through case studies, assignments, and GMP games. The course also gives you the opportunity to network with others who are new to the life sciences.
Sterile 1, Manufacture of sterile medicinal products
Learn about aseptic practices and the safe production of sterile pharmaceuticals
This course provides practical training in aseptic practices, hygiene, and work techniques in classified areas. You will practice cleaning and disinfecting equipment and following the GMP Annex 1 requirements for sterile pharmaceuticals.
GMP 2, GMP in Practice
SImprove production quality through hands-on training
In GMP 2, GMP in Practice, you’ll learn how to participate in self-inspections, handle deviations, and actively improve quality in production. GMP 2 is a natural follow-up to GMP 1, where you mastered the basic rules.
GMP 1, Pharmaceutical Manufacturing
Learn GMP from the ground up—and get off to a great start in the life sciences
You'll gain an understanding of GMP regulations and the role they play in ensuring the production of consistent, high-quality medicines.
Introduction to Qualification and Validation
Become familiar with the principles and concepts of qualification and validation
The course consists of two e-learning modules as preparation. They cover qualification and validation requirements, as well as qualification phases. During the course itself, the relationship between qualification phases, documentation, and qualification tests is reviewed, along with practical tips and tricks for these processes.
Quality Agreements in GxP
Are the company's quality agreements under control?
This course is for anyone who wants to learn everything about quality agreements or simply wants tips on how to improve them so you’re ready for an inspection. Learn what should and shouldn’t be included in the agreement.
GDP Rules – Requirements and Interpretations
Learn how to navigate the GDP rules
This course provides you with a comprehensive overview of the GDP regulations. After completing the course, you will be able to interpret the regulations and assess which requirements are relevant to your business. You will gain a solid foundation for participating in regulatory inspections.
Regulatory Life Cycle Management
Marketing authorizations are in the spotlight
What happens in the Registration Department after the initial marketing authorization is granted?
Understand the principles and requirements for maintaining a marketing authorization for a human medicinal product in Denmark and the EU.
GMP for IT Managers
Understanding Regulatory Requirements for IT in the Life Sciences
Here, we take a close look at the requirements for IT and the operation of computer systems. You’ll gain insight into and a practical understanding of both GMP requirements and their implementation, so you can ensure compliance in the development, operation, and maintenance of IT systems.
This course is essential for IT managers who want to master the complex rules and guidelines.