How to depyrogenate sterile products by rinsing
Learn what depyrogenation by rinsing is, why is depyrogenation needed and how to use rinsing for a medical device’s or product’s endotoxin removal.
Learn what depyrogenation by rinsing is, why is depyrogenation needed and how to use rinsing for a medical device’s or product’s endotoxin removal.
Learn how to select and create endotoxin indicators for depyrogenation validation processes and regulatory testing.
Learn the differences between contract testing and contract manufacturing and how they can both ease medical device manufacturing and regulatory testing.
Learn about sterilization testing and validations and how autoclaves use steam to sterilize medical devices or other medical products.
Learn what sterilization validations are and how to validate steam sterilization processes for your medical device or medical product.
Learn what contract testing is and the benefits of using contract testing organizations to support you with medical device regulatory testing.
Learn what sterilization validations are and how to perform sterilization validations for radiation sterilized medical devices or medical products.
Learn what medical devices are and aren’t regulated by the United States Food and Drug Administration (FDA) and how the FDA classifies medical devices.
Learn about the importance of medical devices in healthcare, and their current benefits as well as facility and patient-related risks regarding its usage.
Learn how microbiology testing is performed and how it relates to testing your nutritional and dietary supplements.