Slow, unglamorous work, and no result that is not confirmed twice.
Titreon started small and stayed small: two analytical chemists tired of research-compound certificates no one could check, building a method library and a review standard for a circle of researchers who found them by word of mouth, with reports that went out as plain PDFs and initials at the bottom before there was ever a website or a brand.
The rule that matters most came out of that period: every peptide assay is confirmed against a second, orthogonal method before any certificate is issued, and every certificate carries the raw data behind it. Methods are validated against USP and pharmacopeial reference standards, and Titreon’s own ISO/IEC 17025 accreditation is in progress.
Small on purpose.
A handful of analytical chemists, a quality lead, and one person who answers the emails and ships the sample kits. That is the whole company, and we intend to keep it that size.
Marcus L.
Years in Bay Area contract labs before Titreon. Co-built the method library behind every Titreon certificate.
Devi R.
The other half of the founding pair, and the reason the method library is what it is.
Finn C.
Close to two decades in pharmaceutical and bioanalytical QC. The reason our SOPs and acceptance criteria exist in their current form, with sign-offs at every stage.
Brennan C.
Owns release. No certificate goes out until it has been reviewed against acceptance criteria under the Titreon quality system.
The rules we built the hard way
We route testing to independent lab partners
Titreon outsources its analytical testing to independent lab partners. We route each sample to the lab partner best suited to the work, review the returned data, and issue the certificate under our own quality system. We do not publicly name our lab partners.
Two methods, every time
Every batch gets full method validation, not a single-injection screen, and every assay is confirmed against a second, orthogonal method before it is released.
We hand you the raw data
Every certificate includes the chromatographic and spectral data behind the result, so you can check our work instead of taking our word for it.
Validated, and honest about the rest
Our methods are validated against USP and pharmacopeial reference standards, and our testing is carried out by independent lab partners. Our own ISO/IEC 17025 accreditation is in progress. Our SOPs are available on written request.
We do not compete on price
Titreon costs more than the bargain COA mills, because full validation costs more than a single injection. If the cheapest certificate is the priority, we are not the right lab for you.
Independence & compliance
Titreon Analytical is a testing laboratory only. We do not manufacture, sell, supply, endorse or recommend any product we test, and nothing we publish is medical, clinical or dosing advice. Titreon outsources its analytical testing to independent lab partners: samples are routed to the partner laboratory best suited to the work, and Titreon reviews the returned data and issues the certificate under its own quality system. We do not publicly name our lab partners. Methods are validated against USP and pharmacopeial reference standards; Titreon’s own ISO/IEC 17025 accreditation is in progress. All materials referenced are for laboratory research use only and are not for human or veterinary use. Any decision made on the basis of a result is taken at the reader’s own risk.
Work with a lab that
sweats the details.
Send a sample, or verify a certificate you already hold.