Good Manufacturing Practices (GMP) For Pharmaceutical industry Training Course
Course Overview
What you'll learn
Upon completion of this course, learners will be able to:
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Discuss the general principles of GMP.
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Be aware of the requirements for:
•Personnel, training, sanitisation and cleaning;
•Deviations, returns, self-inspections, documentation;
•Facilities, equipment, qualification;
•Production, process controls, labelling and packaging;
•Laboratory controls, control of components, containers and closures, finished drug product controls and acceptance criteria.
Who This Course Is For
This course is designed for anyone involved in the development, implementation and management of GMP for the Pharmaceutical industry, particularly relevant for those organisations that produce pharmaceutical products and need to become compliant to GMP.
About this course
All manufacturing personnel must receive initial and ongoing training in the theory and practice of GMP. Everyone who works in a processing, quality control, packaging, or warehouse environment for a pharmaceutical or biotechnology company, or one of their contractors, must understand why GMP is important, how it applies to them, and how to comply with it. This course provides an introduction in the basics of GMP.
This course discusses what GMP is and why it is important, the main principles of GMP and how different departments function together with protecting quality, safety and efficacy of the pharmaceutical products.
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