Questions

Not yet. Leave your email in the form on the homepage and we’ll notify you when sample intake opens, with the test panels, pricing, and submission instructions.

Pricing is not finalized. We’re considering single-vial testing and other options. Tell us what would be useful to you in the form on the homepage. Minimum quantities and turnaround times will be published before intake opens.

We’ll publish the accepted compound list and sample requirements when intake opens. The compound shown in the illustrative report is an example, not a confirmation that it will be accepted.

Yes. Bacterial endotoxin screening is part of our planned launch offering, alongside HPLC purity testing. Endotoxin screening is a separate assay and does not replace sterility, heavy-metal, or broader microbial testing.

No. A lab result answers the specific questions covered by the tests performed. It does not establish safety for human use, determine an appropriate dose, or replace medical advice. Endotoxin screening is also different from sterility testing.

For background: FDA guidance on endotoxin testing (PDF).

A searchable results library is under consideration. No public library is available today. The planned service uses specimen identifiers; it does not test human specimens or collect personal health information.

No. The laboratory holds no position in any compound it measures and supplies none.

A result describes the submitted sample. It does not certify a vendor, a lot beyond the one tested, or future production.