[White Paper] Primary Validation of the Growth Direct Bioburden System and Media

 

EuPharm Rev 5.1.6 Staistics for BB-1 cover page border

In the USP Ch <1223>, the Growth Direct technology is classified as an automated compendial method, requiring only a verification of the counting method followed by a method suitability study. This paper describes the validation methods performed for bioburden test application using Growth Direct system and associated consumables. Experimental data obtained has been analyzed using statistical methods in accordance to EP and USP.


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