Standard peptide analysis: 5-10 business days after receipt and acceptance. Timing for other methods is confirmed in the quote.
How this analysis works
LAL endotoxin testing is $199 CAD per sample ($189 CAD at three or more) and reports endotoxin in the tested preparation. The standard method is kinetic chromogenic LAL under the USP <85> framework; recombinant factor C under USP <86> can be requested instead. It can be ordered alone or added to a panel, but it does not replace sterility testing.
Interfering matrices may require dilution or suitability work.
Acceptance criteria must be supplied or agreed in advance.
What to submit
Matrix and reconstitution details are required
Do not ship liquids unless explicitly approved
Sample quantity is confirmed during feasibility review
Reading the result
Read the endotoxin result with its unit, reporting limit, dilution and sample basis. A specification must be agreed before a result can be interpreted as meeting a particular requirement.
Bacterial Endotoxin Testing starts at $199 CAD per accepted sample, excluding tax and shipping. Scope and the final price are confirmed before you mail anything. Volume rates apply from three samples carrying this test in one request.
02
How long does this test take?
Timing is confirmed during scope review. Reference-material availability, sample preparation, method development or contract laboratory work can affect the schedule. Shipping time is additional.
03
Does an endotoxin result establish sterility?
No. Endotoxin testing assesses bacterial endotoxin response. It does not replace a sterility test or establish that a sample is safe for use.
04
Can endotoxin testing share the vial used for peptide analysis?
Possibly, subject to sample quantity, preparation and method suitability. Shared-vial acceptance is confirmed before you ship; do not assume one vial is sufficient for every test.
05
Why does the reporting limit depend on the sample?
Sample interference can require dilution or additional suitability work. Read the reported limit and preparation basis with the result rather than comparing unlike units or dilutions.
Technical references
These sources explain the analytical concepts. They do not certify CPT or validate a particular sample result.
