GMP is that part of Quality Assurance which ensures that pharmaceutical products are consistently manufactured to the quality standards appropriate to their intended use and as required by a marketing authorisation or product specification. Manufacturers' compliance with GMP legislation is a requirement of approval of regulatory submissions. Manufacturers are subject to inspection and audit by regulatory authorities. Non-compliance with GMP requirements can have significant commercial consequences for a pharmaceutical company. In an area that is subject to stringent enforcement of the regulatory requirements, this module provides continually updated guidance on GMP requirements.


Who will benefit from this module?
All staff involved in manufacturing and quality control in pharmaceutical companies or their suppliers need to be up to date with current GMP requirements. They will find this course an invaluable guide and reference source.