Alconox Inc. White Papers

These technical white papers and informative handbook will provide you with beneficial insights and useful tools. If desired, please select the white paper that best meets your needs.

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- Applications in Medical Device Manufacturing
  The use of aqueous cleaning in medical device manufacturing can provide numerous benefits in terms of efficacy, minimal surface contact and reduced residue potential, and easier cleaning validation.
- Applications in Pharmaceutical Manufacturing
  The use of aqueous cleaning in pharmaceutical manufacturing can provide numerous benefits in terms of effectiveness, minimal surface residue, and easier cleaning validation.
- Cleaning and Monitoring Procedures
  Getting the best results from any cleaner requires proper mixing and cleaning procedures. This whitepaper includes mixing directions for each type of Alconox Inc. aqueous cleaning detergent. It also describes methods for monitoring cleaner performance.
- Cleaning Validation for Pharmaceutical Manufacturing Cleaning
  validation is a necessary and time-consuming part of manufacturing pharmaceuticals. This white paper outlines the basics of cleaning validation and discusses the support services you should seek from your critical cleaning products supplier to optimize your cleaning validation process.
- Cleaning Validation for Medical Device Manufacturing
  Cleaning validation or verification is a necessary regulatory compliance step in medical device manufacturing and reprocessing. This white paper outlines the basics of cleaning validation and how the cleaner manufacturer can help simplify and speed up the process, as well as support ongoing maintenance of the validated or verified state.or verified state.
- Cleaning Validation References
  A cleaning validation involves testing for acceptable residues on pharmaceutical manufacturing or medical device surfaces. This white paper provides references for what is required including: residue identification and detection method selection, sampling method selection, setting residue acceptance criteria, methods validation and recovery studies, as well as writing a procedure and training operators.
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