Ready for Inspection|company
Be Ready for Your Next Regulatory Inspection
Understand the requirements, roles and appropriate conduct before, during and after an inspection. Employees receive practical advice to help your company approach the inspector calmly, knowledgeably and professionally.
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.
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.
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 the 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 everyday 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
Get the Basics of Qualification and Validation
Gain an understanding of the requirements for qualification and validation when new equipment or processes are introduced in pharmaceutical manufacturing – and learn how to ensure traceability from requirements to testing.
From Compliance to a Culture of Quality|company
When Quality Becomes More Than Compliance
Learn how to translate GMP into everyday practice so that you not only comply with requirements, but also actively contribute to a strong quality culture that supports patient safety, data integrity and collaboration.
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 cases that would benefit from dedicated time together to gain insight and capture important learning?