What is the difference between ISO 22000 and 13485 ?

Title: What is the difference between ISO 22000 and 13485? A comparison for food safety industries

ISO 22000 and ISO 13485 are both certifications that are highly regarded in the food safety industry. These two certifications are designed to ensure that a company's quality management system is up to standard, and that they are able to meet the necessary requirements for food safety. However, some may wonder what the main differences are between ISO 22000 and ISO 1348In this article, we will provide a comprehensive comparison of these two certifications and highlight their unique features and applicability in the food safety industry.

ISO 22000: Ensuring Food Safety

ISO 22000 is an international standard that is designed specifically for the food industry. This standard was developed to ensure that food companies have a comprehensive quality management system in place that meets the requirements of food safety legislation and regulations. The standard is divided into ten parts, each of which covers a different aspect of the food safety management system.

One of the main differences between ISO 22000 and ISO 13485 is the scope of their requirements. ISO 22000 is focused specifically on food safety, while ISO 13485 is focused on medical devices. This means that companies that are in the food industry will be more heavily impacted by the requirements of ISO 22000, while those in the medical device industry will be more heavily impacted by the requirements of ISO 13485.

Another difference between the two standards is the level of detail they require. ISO 22000 is a more general standard that is designed to provide a framework for a quality management system, while ISO 13485 is a more specific standard that is designed to provide detailed requirements for a medical device quality management system.

ISO 13485: Ensuring Medical Devices Safety

ISO 13485 is an international standard that is focused on ensuring the safety of medical devices. This standard is designed to be specific to the medical device industry and is divided into ten parts, each of which covers a different aspect of the medical device quality management system.

ISO 13485 is highly focused on ensuring the safety of medical devices and is therefore designed to be more detailed and specific than ISO 22000. This means that companies that are in the medical device industry will be more heavily impacted by the requirements of ISO 13485, while those in the food industry will be more heavily impacted by the requirements of ISO 22000.

Comparison of ISO 22000 and ISO 13485

In conclusion, ISO 22000 and ISO 13485 are both important certifications that are designed to ensure quality and safety in different industries. While they may seem similar, they are distinct certifications that are tailored to different industries and have distinct requirements. Companies that are in the food safety industry will be more heavily impacted by the requirements of ISO 22000, while those in the medical device industry will be more heavily impacted by the requirements of ISO 13485.