Pharmaceutical companies manufacture different types of drugs for different diseases. Good manufacturing practice (GMP) and good laboratory practice (GLP) are the principal criteria and guidelines that pharmaceutical companies need to follow in manufacturing. Guidelines and criteria are prepared and disseminated by the Food & Drug Administration (FDA) of America. The FDA website provides a generous database of information for consumers and pharmaceutical professionals regarding drugs and their manufacture or usage.

One of the principal GMP requirements in pharmaceutical manufacturing is the necessity for the accurate identification of drugs and assurance that accurate patient information is provided.

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