impuritylab.com

Quality and compliance

What arrives with every standard

Documentation is the product. Everything below is issued per lot, not assembled on request.

dual
ISO 17034 accreditation — CNAS and ANAB est.
per lot
COA issued against the shipped lot
3 routine
HPLC, LC-MS and NMR data where applicable
2 days
Target response time on technical requests

Documents

Certificate of analysis

Identity, purity, method, lot number, re-test date and the analyst sign-off for the batch that ships.

Safety data sheet

Issued in the format your EHS team expects, with transport and disposal classification.

Analytical data

Chromatograms and spectra as raw files where you need to reprocess, not only as images in a PDF.

Handling and traceability

Lot traceability

Every vial carries a lot number that maps back to the batch record and its certificates.

Custom synthesis documentation

Made-to-order compounds ship with the same documentation set, plus the synthesis route summary.

Questions after delivery

Technical questions go to the same inbox as quotes and are answered by the person who released the lot.

Accreditation and capability statements on this page are demo placeholders. Confirm the exact scope wording with the quality team before this goes live.
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