Good Manufacturing Practice (GMP)

Good Manufacturing Practice (GMP) is described by the World Health Organization as a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects.

GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made.

The manufacture of medicinal products relies upon people and the establishment and maintenance of a satisfactory system of quality assurance. GMP is an essential component of such a system of quality assurance. It therefore follows alll personnel should be aware of the principles of GMP that affect them.

The Essential Elements of GMP

This is a free course that describes the basic requirements of GMP. You will be able to access the course by registering on our eCampus website. Please see the GMP Course page which describes the procedure for obtaining your unique login and instructions on how to complete the course.

PROVEN COURSE MATERIAL: More than 16,000 people have already taken Version 1 of this course.


Version 2 of the GMP Course is currently being updated to enable the course to run on mobile and tablet formats, as well as standard browsers and is not available at present.

Please call back soon.




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