Quality Control on Media

Dry Powder Media

Dry Powder Media are physically tested for osmotic effects and pH.
Osmolality is established by means of the Freezing Point Method, following European Pharmacopeia EU Ph. 2.2.35.
Biowest analyses representative samples of the mixture's chemical composition and homogeneity to verify the concentration of glucose or sodium.
We also perform a chromokinetic - quantitative test - method D of the European Pharmacopoeia EU Ph. 2.6.14 to determine and quantify endotoxin levels.

 

Liquid Media

A biological performance test is done on cell lines corresponding to their particular medium.
The endotoxin level is also tested by a Chromo Kinetic test, a chromokinetic - quantitative test - method D of the European Pharmacopoeia EU Ph. 2.6.14.
Liquid Media are tested for sterility, pH and osmolality (following European Pharmacopeia EU Ph. 2.2.35).

 

Intended Use

label_scientific

These products are intended for research applications.
It is the end user's responsibility to qualify these products for their specific application.
These products are not for diagnostic use.
Their safety and efficiency have not been established for diagnostic or other clinical uses.

 
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