Top 4 Cleaning Validation Challenges In 2022 For Reusable Devices
Learn about the top challenges medical device companies face when performing cleaning validations for reusable medical devices.
Learn about the top challenges medical device companies face when performing cleaning validations for reusable medical devices.
Learn calculations and most probable number equations for alternative method equivalency testing for microbiological testing and medical product testing.
Learn the differences between cleaning validations and sterilization validations for regulatory testing of your medical devices.
Learn about corrosion resistance for reusable medical devices exposed to gamma radiation and ethylene oxide sterilization processes.
Find here Spaulding classification guidelines for reusable medical devices regarding cleaning validations and sterilization validations.
Learn about the USP 81 zone of inhibition test for antimicrobial agents, materials, and coatings on or within medical products and cylinder-plate assays.
Learn about method suitability and equivalency testing requirements for new medical devices, products, and alternative test methods.
Learn about environmental controls, pharmaceutical products, and the top nonsterile manufacturing processes for medical devices and products.
Learn about the minimum filling requirements for creams, gels, lotions, ointments, pastes, powders, aerosols, foams, and sprays.
Learn how to perform USP 1072 disinfectant challenge testing for cleaning validations to ensure your medical device or product meets FDA guidelines.