Carrier Tests To Assess the Effective Sporicidal Concentration of a Liquid Chemical Disinfectant for a Sanitization Program

References

1. 1.↵
   1. Agalloco J.,
   2. Carleton F. J.

   1. Haberer K.

   Cleaning and Disinfection in the Control of Pharmaceutical Cleanrooms. In Validation of Pharmaceutical Processes, 3rd ed.; Agalloco J., Carleton F. J. Eds.; CRC Press, Inc.: Boca Raton, FL, 2007; pp 303–316.
2. 2.↵
   EudraLex, Vol. 4, Good Manufacturing Practice (GMP) Guidelines, Annex 15: Qualification and Validation. European Commission, 2001.
3. 3.↵
   Pharmaceuticals CGMPs: Guidance for Industry. Sterile Drug Products Produced by Aseptic Processing. U.S. Department of Health and Human Services, FDA, 2004.
4. 4.↵
   Disinfectants and Antiseptics. In USP 30, Chapter 1072; 2006; pp 504–508.
5. 5.↵
   1. Springthorpe V. S.,
   2. Sattar S. A.

   Carrier tests to assess microbicidal activities of chemical disinfectants for use on medical devices and environmental surfaces. J. AOAC Int. 2005, 88 (1), 182–201.

   OpenUrlPubMed
6. 6.↵
   1. Sartain E.

   The ABCs of disinfectant validation. CleanRooms 2005, 19, 23–27.

   OpenUrl
7. 7.↵
   1. Tidswell E. C.

   Bacterial adhesion: considerations within a risk-based approach to cleaning validation. PDA J. Pharm. Sci. Technol. 2005, 59 (1), 10–32.

   OpenUrlAbstract/FREE Full Text
8. 8.↵
   1. Halls N.

   Disinfectant. In Essential Microbiology for QP Candidates; PDA: Bethesda, MD, 2007; pp 205–218.
9. 9.↵
   1. Tomasino S. F.,
   2. Hamilton M. A.

   Comparative evaluation of two quantitative test methods for determining the efficacy of liquid sporicides and sterilants on a hard surface: a precollaborative study. J. AOAC Int. 2007, 90 (2), 456–464.

   OpenUrlPubMed
10. 10.↵
    1. Tomasino S. F.,
    2. Pines R. M.,
    3. Cottrill M. P.,
    4. Hamilton M. A.

    Determining the efficacy of liquid sporicides against spores of bacillus subtilis on a hard nonporous surface using the quantitative three step method: collaborative study. J. AOAC Int. 2008, 91 (4), 833–852.

    OpenUrlPubMed
11. 11.↵
    1. Strickland L.

    Disinfection begins with proper selection. CleanRooms 2008, 22, 26–31.

    OpenUrl
12. 12.↵
    1. McDonnell G. E.

    Antisepsis, Disinfection, and Sterilization: Types, Action, and Resistence; ASM Press: Washington, DC, 2007.
13. 13.↵
    1. Sutton S. V.,
    2. Proud D. W.,
    3. Rachui S.,
    4. Brannan D. K.

    Validation of microbial recovery from disinfectants. PDA J. Pharm. Sci. Technol. 2002, 56 (5), 255–266.

    OpenUrlAbstract/FREE Full Text
14. 14.↵
    1. Johnston M. D.,
    2. Simons E. A.,
    3. Lambert R. J.

    One explanation for the variability of the bacterial suspension test. J. Appl. Microbiol. 2000, 88 (2), 237–242.

    OpenUrlPubMed
15. 15.↵
    EudraLex, Vol. 4, Good Manufacturing Practice (GMP) Guidelines, Annex 1: Manufacture of Sterile Medicinal Products. European Commission, 2003.