GMP Essentials for Clinical Operations Staff
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About this course
Reasons to attend
This ½-day GMP Essentials course is especially designed for clinical operation teams, to get an understanding of the Good Manufacturing Principles (GMP) in relation to management of Investigational Medicinal Product (IMP) in the framework of a clinical trial.What's included?
- Documents and materials related to this course are included
- Globally recognised certificates awarded after test completion
Course schedule
- Half Day face-to-face training: 09h00-12h30
Course Description
During the brief introduction on the manufacturing of clinical trial material, the participants will get an overview at a glance on the processes before the material is received in the clinic.The half day course will discuss the European GMP on a high level, the importation and packaging of IMP’s and the two-step approach as applied for the release of the material for clinical trials. Next to that a brief introduction will be given on the release and shelf life testing of IMP’s and how this influences the labelling strategy for the IMP.This GMP Essentials course is designed as an optional add-on to our Clinical Project Management course but can also be followed independently.Programme highlight
- Introduction to GMP
- Import, Packaging and Distribution of IMPs
- Clinical Release (Workshop)
- Testing and Release of IMP
Learning objectives
- Get an understanding on the basic principles of Good Manufacturing Practices
- Get an understanding of the role of the Qualified Person in the manufacture of clinical trial materials
- Get an understanding on how the packaged clinical trial material gets to the clinic before trial commencement
Who should attend
Clinical Operations staff who need to know the basics on how IMP is manufactured and managed in the context of a clinical trial.
Competencies
This GMP Essentials course covers competencies that are part of the ECCRT Competency Framework
- Scientific Concepts & Research Design (0)
- Ethical & Participants Safety Considerations (0)
- Investigational Product Development and Regulation (3)
- Clinical Studies Operations (GCPs or ISO 14155) (0)
- Study and Site Management (0)
- Data Management and Informatics (0)
- Leadership and Professionalism (0)
- Communication (0)
- Teamwork (0)
- Business acumen (0)
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