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ORA FAQs
What is GMP?

Food and Drug Administration (FDA) Good Manufacturing Practices (GMP) have been defined as "the part of quality assurance which is aimed at ensuring that products are consistently manufactured to a quality appropriate to their intended use." GMP standards are the minimum methods to be used in, and the facilities or controls to be used for, the manufacture, processing, packing, or holding of a drug or medical device to ensure that the drug or device meets safety, identity, strength, quality, and purity characteristics that it purports or represents to possess.


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