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.

A Current Good Manufacturing Practices (GMP) certificate verifies and certifies that standards for a successful Hazard Analysis Critical Control Point (HACCP) food safety program are being followed. The FDA uses it to verify that foods are safe for customers and to “improve food safety control at all phases of manufacturing, processing, distribution, and consumption.”