Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
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What Exactly is GMP?
Good manufacturing practice is a critical system used to ensure that drugs and medical devices are produced according to the highest quality standards. Although the overarching framework of GMP is set up by the FDA, continuously adhering to the most stringent levels of quality control demands a robust set of internal protocols for ensuring that every link in the manufacturing chain is above reproach from a quality assurance perspective. Essentially, GMP is a pharmaceutical quality benchmark that is achieved by setting an extremely high bar for ongoing QA/QC.
Understanding GMP Pharma Guidelines
As most GMP principles are relatively open-ended, the onus is on the pharmacy
