GDP for Management
Get a clear understanding of your responsibilities
Management is responsible for the company's quality system. Participants will gain a solid understanding of current EU GDP regulations, with a particular focus on management's responsibilities and tasks.
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.
Basic GDP
Safety and Quality in the Distribution of Medicines
Learn the rules so you can help ensure the quality of medicines throughout the supply chain. We’ll go over the rules so you can apply them in practice.
Tablet Manufacturing
Gain both practical and theoretical knowledge of the entire tablet manufacturing process
In this course, you will learn about all the parameters that affect tablet manufacturing.
The course also provides you with hands-on experience with the tablet manufacturing process.
You will learn to work independently, follow procedures, and complete documentation in accordance with GMP.
From Compliance to a Culture of Quality|Company
When Quality Goes Beyond Compliance
Learn how to implement GMP so that you not only meet the requirements but also actively contribute to a strong culture of quality that enhances patient safety, data integrity, and collaboration.
Learn from Your Own Cases and Establish a Shared Direction|Company
Join a facilitated workshop where you’ll set aside time together to understand and learn from your own cases
Do you have deviations, SOPs, audit findings, collaboration challenges, or other production-related issues that call for time spent together to gain insights and important lessons?
Qualification and Validation – From Requirements to Testing | Company
Master the basics of qualification and validation
Understand the requirements for qualification and validation when new equipment or processes are to be used in pharmaceutical manufacturing—and learn how to ensure traceability from requirements to testing.
GMP – From Legal Requirements to Everyday Practice | Business
Understand the legal requirements in your daily work
Do you understand why you do what you do?
And do you know how much of a difference each person’s efforts make to the final drug?
Requirements for Production Facilities and Equipment in a Controlled Environment|Company
Learn how facilities and equipment support product quality
Employees gain insight into GMP requirements for facilities and equipment and an understanding of how facilities and equipment support quality, compliance, and patient safety.
GMP Documentation Management | Company
Good Documentation Practices: Clear, Accurate, and Traceable
Documentation is a key element of GMP and crucial for patient safety.
It’s rarely the major errors that cause problems.
Often, it’s the small details in the documentation.
Master good documentation practices and avoid mistakes in your daily work.