GMP is short for Good Manufacturing Practice and is commonly used also for Quality Management systems related to manufacture of medicinal products/pharmaceuticals. Other organisations within the Life Science industry, e.g. developers of IVDs and Medical devices may have to follow similar requirements. In this introductory course, you will get an overview of the requirements and guidelines that governs quality management related to manufacturing. The course is based on requirements for pharmaceuticals but regulatory requirements and ISO 13485 for medical device quality systems is briefly covered.
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This course is available as an In-House Training course. Let us know if you wish to customize a course or if you are a large group with the same requirements.
Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.
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