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Type   Document Title
  Steam Sterilisation: The importance of air removal and verification

Understand the importance of air removal and verification including test details, regulations and standards, and risk mitigation for steam sterilization.

  Scientific Justification for Monitoring Indirect Product Contact Surfaces

Whether it is a solely visual inspection or a combination of visual inspection with microbial and residue removal, your level of monitoring should depend on the type of indirect product contact surfaces.  Learn more in this article.

  Understanding H2O2 For Vaporized Hydrogen Peroxide (VHP)

Selecting the appropriate hydrogen peroxide to use with your equipment will help ensure that your equipment and process performs optimally.

  Residue removal in cleanrooms: A regulatory overview

With various sources of residue generation within your cleanroom, an effective cleaning and disinfection program is crucial to prevent microbial and other cross-contamination. Learn more in this article.

  The Advantages of Decontaminating with Vapor Phase Hydrogen Peroxide

Learn about the Advantages of Decontaminating with Vapor Phase Hydrogen Peroxide used in processes where traces of toxic substances are unacceptable.

  Visual Inspection Practices of Cleaned Equipment

Regulatory and compendial guidelines require that manufacturers confirm process equipment is visually clean following a cleaning operation.

  Guide to implementing a VHP system for facility biodecontamination

Vaporized hydrogen peroxide biodecontamination systems can be installed and integrated into a plethora of cleanrooms or suits.

Technical Tips   Importance of Air Removal in Autoclave Steam Sterilization Processes

The removal of air is very important in an autoclave steam sterilization process.

Technical Tips   Services to Consider When Validating Your Equipment

Validation is an essential part of your operation. Make sure your equipment performs up to your standards and ensure compliance with industry regulations with validation services from STERIS.

Technical Tips   When Risk is Not an Option: A Look at FDA 483's

Risk management involves both the assessment and minimization of risk.

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