The Pharmig guide to disinfectants has been completely revised and re-written to provide a roadmap to regulatory compliance for cleaning and disinfection.
The new text will walk the user through the steps needed to design, validate, and implement an effective cleaning and disinfection programme. Including:
- Identifying and assessing risks associated with cleaning and disinfection
- User requirements for cleaning agents and disinfectants
- Supplier qualification
- Disinfectant efficacy testing and validation
- Controls for routine use – including application methods, in-coming QC testing, and periodic review of the programme
The reference is:
Kirkham, R., Guardi, L., Moorwood, K. and Sandle, T. (2022) A guide to cleaning and disinfection of pharmaceutical facilities – a road map to regulatory compliance, Pharmig, Stanstead Abbotts, UK
To order see: Pharmig
Posted by Dr. Tim Sandle, Pharmaceutical Microbiology Resources (http://www.pharmamicroresources.com/)
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