Pharma, device & biotech

Talk to a scientist,
not a queue.

Method development, validation, release, and stability testing for drug products, devices, and biologics. You work directly with the scientists running your samples, and every result leaves the lab QA-reviewed and ready for an audit.

AccreditationISO/IEC 17025ANAB certificate AT-2851
RegistrationFDAFEI 3008810414
CompliancecGMP · Part 11Plus GCP and GCLP
DEA licenseI to IIIControlled substances
What we do

From method development to batch release.

What you get

This is what lands in your inbox.

Not a summary. A complete, QA-reviewed package your auditors can follow line by line.

1Criteria set before testing. Acceptance criteria come from the protocol, not after the fact.
2Every peak labeled. Representative chromatograms with retention times.
3Result next to the requirement. You see the number and the conclusion together.
4Signed off by QA. An independent quality review on every report. Raw data under Part 11.
Selected work

Real problems. Solved.

A few we can talk about. Client names stay confidential.

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Send a sample

Bring us the problem. We'll bring the method.

Pick what you're sending and we'll take it from there.