Quality Assurance of AI in GxP
Get a unique opportunity to understand, evaluate, and implement AI solutions in a GxP environment
Explore artificial intelligence (AI) from a non-technical perspective, with a focus on quality and implementation. This course is designed for those who want a broad understanding of AI, with a special focus on quality, validation, and implementation.
Robust SOPs—Your Key to Compliance | Business
Learn how to write SOPs that are easy to understand and support compliance
Write SOPs that are read, understood, and followed.
In this course, employees will learn common tools for making instructions clearer, more practical, and easier to follow in real life.
Mastering GMP Inspections
Gain practical tools to prepare for, conduct, and follow up on regulatory GMP inspections
This course provides practical guidance on how to prepare your organization, manage the inspection process, and respond effectively after the inspection. A key strength of the course is the combination of practical industry experience and direct regulatory insight from an experienced GMP inspector at the Danish Medicines Agency.
Data Integrity – IT and GMP
Help ensure that the company complies with the rules
Are you ready to master the data integrity requirements for GMP-regulated IT systems? Whether you’re a practitioner, system owner, or QA specialist, this course is designed to equip you with strategies and skills in IT and data integrity.
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.
Pharmaceutical Water Systems: Theory and Practice
Design, commissioning, operation, and maintenance of pharmaceutical water and pure steam systems
You will gain insight into regulatory requirements, guidelines, and relevant GMP principles, which will ensure optimal operation and quality of your pharmaceutical water and steam systems. This course combines theory and practice to provide you with in-depth insight into how to effectively manage, monitor, and maintain these essential systems.
Ready for an IT audit
Know the requirements, and look forward to inspections by the authorities
This course will enable you to handle regulatory inspections of IT systems. After completing the course, you will be familiar with the requirements and strategies for IT validation. You will be able to present your validation to the authorities, helping them gain confidence in your approach to IT compliance.
Control of GMP Documentation
Good Documentation Practices: Clear, Accurate, and Traceable
Documentation is a key element of GMP and crucial for patient safety.
It’s rarely major errors that cause problems. Often, it’s the small details in the documentation.
Get a handle on good documentation practices and avoid mistakes in your day-to-day work.
From Compliance to a Culture of Quality
When Quality Goes Beyond Compliance
You’ll learn how to implement GMP so that you not only meet the requirements but also actively contribute to a strong quality culture that enhances patient safety, data integrity, and collaboration.
From Compliance to a Culture of Quality
When Quality Goes Beyond Compliance
You’ll learn how to implement GMP so that you not only meet the requirements but also actively contribute to a strong quality culture that enhances patient safety, data integrity, and collaboration.