AAMI ST98 outlines expectations for validating the cleaning process for devices before clinical use. See how it shapes study design, testing, and documentation.
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Press Releases
A Look at IQ, OQ, and PQ for Medical Equipment
IQ, OQ, and PQ confirm that medical equipment is installed correctly, runs within expected limits, and performs reliably. This guide breaks down each stage.…
Steam Sterilization Cycle Development: How It Works
Build clearer steam sterilization instructions with cycle development. Features of reusable devices shape cycle settings, testing, and documentation.…
Selecting Simulated Use Soils for Testing
Reusable devices need soil challenges that match their use and design. Build a stronger cleaning validation study with realistic soil testing.…
Why Autoclaving Is a Common Sterilization Procedure
Reliable sterilization protects patients, samples, and reusable tools. See why autoclaving is a common sterilization procedure in medical and research settings.…
Medical Device Design Validation vs. Design Verification
A well-designed medical device is reliable, aligns with needs, and fits workflows. Validation and verification confirm that device designs meet requirements.…