Basic GMP for New Operators|company
Get New Operators Ready to Begin Work in Your Pharmaceutical Manufacturing Environment
This course is a condensed two-day program designed for new operators in your organization.
It provides a basic understanding of GMP requirements and the requirements that apply to working in pharmaceutical manufacturing. At the same time, employees gain a common foundation for their further training within the organization.
Appendix 1 – Aseptic Manufacturing|company
Understand the Requirements for Sterile Medicinal Products and Learn How to Implement Them in Your Organization
Sterile medicinal products place extremely high demands on the environment, equipment, processes, and behavior.
This company-focused course provides employees with an overview of Annex 1 and enhances their ability to assess, document, and prevent contamination in their daily work.
Robust SOPs – Your Key to Compliance|company
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 gain practical tools to make instructions clearer, more useful, and easier to follow in practice.
The Effective Support Professional|Company
Strengthen Your Role in Collaboration with QA, Operations, and Management
As support professionals, employees need to be able to act professionally and apply their professional expertise—even in challenging situations.
GMP Documentation – Get It Right|company
Good Documentation Practices: Clear, Correct, and Traceable
Documentation is a key element of GMP and essential for patient safety.
It is rarely major errors that cause problems. More often, it is the small details in the documentation.
Get to grips with good documentation practices and avoid errors in your daily work.
GMP – From Regulatory Requirements to Everyday Practice|company
Understand Regulatory Requirements in Your Everyday Work
Do you understand why you do things the way you do?
And do you know how much of a difference your individual contribution makes to the finished medicinal product?
Qualification and Validation – From Requirements to Testing|company
Learn the Basics of Qualification and Validation
Gain an understanding of the qualification and validation requirements when new equipment or processes are introduced in pharmaceutical manufacturing—and learn how to ensure traceability from requirements to testing.
Learn from Your Own Cases and Create a Shared Direction|company
Take part in a facilitated workshop where you set aside dedicated time to understand and learn from your own cases.
Do you have deviations, SOPs, audit findings, collaboration challenges, or other production-related issues that would benefit from setting aside dedicated time together to gain insight and identify key lessons?
From Compliance to a Culture of Quality|company
When Quality Is More Than Just Compliance
Learn how to apply GMP in everyday practice so that you not only meet requirements but also actively contribute to a strong quality culture that supports patient safety, data integrity, and collaboration.
Good Documentation Practice|company
Effective GMP Documentation in Your Organization
Gain a clear understanding of the regulatory requirements for proper GMP documentation and learn how to correctly complete and make corrections to batch documentation in a GMP-regulated environment.