uring Processes (cGMP) and
complying with FDA Guidelines for Class I Medical Devices, Mediatech is
certified under ISO 13485:2003 and compliant with ISO 17025:2001.
Mediatech's facility design and Quality Assurance Systems guarantee low
endotoxin levels for both liquid and powdered products and meets the most
rigid Sterility Assurance Levels for liquid products. All cellgro(R) basal
media and salt solutions must test negative for mycoplasma prior to
release. For more information visit http://www.cellgro.com.
Contact: Julie Fry, International Marketing Associate I, Mediatech,
Inc. 1.800.CELLGRO or jfry@cellgro.com.