The presence of pyrogen in compounded sterile products can lead to complications for the individual receiving the injection such as shock, fever, altered resistance to bacterial infection as well as other biological effects. Front Range Laboratories offers LAL testing methods to screen your compounded products for the presence of pyrogen. Our Microbiology Department is able to complete pyrogen analysis within a 24 hour period. We are able to help you determine the Minimum Valid Concentration, Maximum Valid Dilution and the Endotoxin Release Limit for your specific product.

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