COA Validator
Validate pharmaceutical COAs before they become quality risks.
PharmaTrust checks document completeness, specifications, analytical results, methods, sample quantities, dates, signatures and internal inconsistencies, then produces a traceable report for expert review.
Five automated analyses every month, free. No card required.
What the analysis gives you
A certificate either supports a decision or it does not. The report says which, and shows its working either way.
Findings you can defend
Each finding carries the requirement it relates to, the evidence observed, the reasoning, the source and version, and the action that closes it.
Refusals, not guesses
Where the certificate does not carry enough evidence to reach a conclusion, the report says so and names what is missing. A confident wrong answer is worse than no answer.
A record that reproduces
Every analysis stores the engine, source versions and rule fingerprint that produced it, so a report from months ago still resolves to the exact basis it was made on.
Three steps
Upload the certificate
A PDF or a scan. Nothing is shared with another customer.
Read the analysis
Findings, open items and the evidence each one rests on.
Decide, or ask for review
Export the report, or request an Expert-Reviewed Analysis.
Who uses it
Pharmaceutical manufacturers
Incoming material certificates checked before release to production.
Importers and distributors
Supplier certificates checked before purchase and before customs.
Laboratories and CDMOs
A consistent second read across analysts and shifts.
Regulatory authorities
A structured, evidence-linked view of a submitted certificate.
Your documents stay yours
Uploaded certificates and the analyses produced from them belong to your organisation and are never pooled with another customer's data. Transport and storage are encrypted, access is role-controlled, and every analysis is auditable.
From the Knowledge Center
What must a certificate of analysis for an API contain?
The elements ICH Q7 expects on a certificate of analysis for an active pharmaceutical ingredient: identity of the material and batch, the dates, every test with its limit and result, and a dated signature from the quality unit with the manufacturer's details.
Retest date or expiry date: what is the difference, and what should a COA show?
The two dates mean different things. An expiry date is the point after which a material should not be used; a retest date is the point at which it should be re-examined. ICH Q7 defines both and says which should appear on a certificate of analysis.
Can a manufacturer rely on a supplier's certificate of analysis instead of testing?
Partly, and only under conditions. US, EU and ICH requirements all allow a supplier's certificate to replace some in-house testing, but each insists on an identity test of every batch, on establishing the reliability of the supplier's results, and on confirming them at intervals.
Validate a certificate now
Five automated analyses every month, free. No card required.