
GMP (Good Manufacturing Practices) guidelines are established to assist and regulate pharmaceutical organizations in the production of unadulterated products. Under a GMP audit, companies must comply with recognized standards in their overall programs and execution related to their grounds, building and equipment; pest control; employee practices; receiving, storage and shipping; plant sanitation; and processing.
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In the pharmaceutical industry, strict standards exist to ensure the safe consumption and manufacture of drugs. TÜV SÜD PSB provides analytical tests to help pharmaceutical companies, healthcare organizations, medical product distributors and procurement agencies meet the necessary requirements for drugs and pharmaceutical products.
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