Environmental Monitoring vs. Sterilization Validation
Learn how environmental monitoring compares to sterilization validations and how these tests relate to regulatory testing for your medical device or medical product.
Learn how environmental monitoring compares to sterilization validations and how these tests relate to regulatory testing for your medical device or medical product.
Learn how to monitor environments for aseptic production and testing processes of your medical devices and your medical products.
What is bioburden testing? Why is bioburden testing necessary? Learn more about these questions, about bioburden testing methods and more.
Looking to determine if your reusable device’s cleaning protocol is robust enough? Use these 6 soil markers to test the cleanliness of your devices.
Learn all about the overkill method and why it is better for you to use it for sterilization validation process of your products.
Appropriate decontamination processes for medical devices must occur to prevent the transmission of disease, especially for reusable devices reprocessed by health care facilities.
The top seven factors that determine the sterility of reusable and one-time use devices alike. A must read for manufacturers writing their instructions for use (IFUs).
Medical device regulations for products sold within the United States of America (USA) do not always equate to the regulations needed for medical devices to be sold within the European Union.