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Microsite, Inc. brings you this unique learning experience in Environmental Monitoring Requirements and Best Practices for Medical Devices and Drugs; Part of Microsite s step-by-step webinar series.
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Who needs new AAMI and ISO:

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Companies involved in the medical device industry, such as manufacturers, distributors, and suppliers, may need to fill out new AAMI (Association for the Advancement of Medical Instrumentation) and ISO (International Organization for Standardization) forms. These organizations set guidelines and standards for quality management systems and product documentation within the industry.
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AAMI (Association for the Advancement of Medical Instrumentation) and ISO (International Organization for Standardization) are organizations that set standards for medical devices and equipment.
Manufacturers and developers of medical devices and equipment are required to comply with the standards set by AAMI and ISO.
To fill out new AAMI and ISO standards, manufacturers need to carefully review the requirements and guidelines provided by these organizations and ensure that their products meet the specified criteria.
The purpose of new AAMI and ISO standards is to ensure the safety, effectiveness, and quality of medical devices and equipment used in healthcare settings.
Manufacturers are required to report detailed information about their medical devices, including specifications, testing results, and compliance with the set standards.
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