ISO (International Organization for Standardization) is an independent, non-governmental international organization that develops and publishes standards for a wide range of industries, including manufacturing and production. These standards are designed to promote international collaboration and ensure consistency in the production and testing of products.
GMP, on the other hand, is a specific set of guidelines and procedures that companies follow to ensure the quality and consistency of their products. It is primarily used in the pharmaceutical, medical device, and food industries, and is considered a critical component of good manufacturing practice.
While ISO and GMP are both focused on promoting quality control and ensuring the safety and reliability of products, they have distinct differences in their scope and objectives.ISO is primarily focused on developing and publishing standards for a wide range of industries, while GMP is specifically focused on the pharmaceutical, medical device, and food industries.
ISO provides a framework for companies to follow when developing and publishing standards, while GMP provides specific guidelines and procedures that companies must follow to ensure compliance with these standards. In other words, ISO is the organization that develops the standards, while GMP is the organization that implements the standards.
In conclusion, while ISO and GMP are both used to promote quality control and ensure the safety and reliability of products, they are distinct entities with different focuses and objectives. ISO is primarily focused on developing and publishing standards, while GMP is specifically focused on implementing those standards. Understanding these differences is essential for companies to ensure they are following the correct guidelines and procedures for ensuring the quality and safety of their products.
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