GMP stands for Good Manufacturing Practice, and it is a word that is used around the world to describe the control and management of pharmaceutical product manufacturing, testing, and overall quality.
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Medical device makers use the 510k premarket notification to legally market a new medical device. This procedure necessitates the submission of technical data to the Food and Drug Administration (FDA) on a prescribed form known as a Premarket Notification (510k) Application
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ISO 13485 is the ISO standard that specifies requirements for a comprehensive quality management system for manufacturers of medical devices. https://ias-certification.com/....iso-13485-training-i

HACCP stands for Hazard Analysis and Critical Control Point. HACCP is a system that identifies critical points in the production chain at which controls can be applied to prevent
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A Quality Management System, also known as ISO 9001:2015, which is one of the most widely used ISO standards across all industry sectors, must be conducted by qualified internal auditors.
https://ias-certification.com/....iso-9001-internal-au