Our resources section contains product literature, technical data, case studies, material safety data, certifications and articles published about STERIS products and solutions.

Search Results

Type   Document Title
Article Reprint   Room Decontamination With Hydrogen Peroxide Vapor

STERIS demonstrates vaporized hydrogen peroxide biodecontamination efficacy in a variety of different pharmaceutical, biotechnology and research room applications.

Case Study   Validation of Cleaning for Research Glassware
This Technical Tip covers validation of the cleaning of glassware used for research purposes in a pharmaceutical or other regulated manufacturing environments.
Sell Sheet   IQ OQ Validation
IQ OQ Validation
Sell Sheet   IQ OQ Validation Spanish
IQ OQ Validation Spanish
Sell Sheet   PQ Validation Service
Article Reprint   Rethinking Cleaning Validation for API Manufacturing

Cleaning validation is a critical component in the manufacturing of pharmaceutical ingredients (APIs) and drug products. This article illustrates new and traditional techniques in designing a cleaning process, ensuring the surfaces are clean and developing rinse solution analysis to continuously monitor cleaning performance. 

The article is published in Pharmaceutical Technology in both the United States and Europe. 

Read the Article - United States (Pages 42 - 54)

Read the Article - Europe (Pages 20 - 32)

Case Study   Prion Inactivation Using a New Gaseous Hydrogen Peroxide Sterilization Process

STERIS demonstrates that use of gaseous peroxide in a standard low-temperature sterilization process may present a useful method of prion inactivation

Article Reprint   Evaluating Surface Cleanliness Using a Risk-Based Approach

STERIS experts, E. Rivera and P. Lopolito, have written "Evaluating Surface Cleanliness Using a Risk-Based Approach" BioPharm International 30 (11) 2017.  This article talks about rinse sample analysis or visual inspection that can be correlated to surface cleanliness to replace surface sampling.

Surface cleanliness is crucial in ensuring that process residue, cleaning agent residue, and bioburden do not adversely affect the safety, quality, and potency of the drug manufactured.

Read more on this topic here on

Data Sheet   Septihol Ready To Use Alcohol Data
Sell Sheet   Spor Klenz Ready to Use Cold Sterilants

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