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GMP (Good Manufacturing Practices) training is a key element of any successful quality assurance program. It involves training staff in the principles and practices necessary for producing safe and effective products and complying with relevant regulations. GMP training typically covers topics such as: understanding regulatory requirements, product safety, cleanliness, documentation, record keeping, quality control and assurance, and risk management.

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ISO 13485 is the ISO standard that specifies requirements for a comprehensive quality management system for manufacturers of medical devices. ISO 13485:2016 was published by ISO on January 1, 2016. Any firm involved in the design, production, installation, or servicing of medical equipment can benefit from ISO 13485 training courses to better understand and apply quality management requirements.
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