Platform
One foundation, built for documents that carry risk
Pharmaceutical compliance runs on documents. The same questions repeat across all of them: is this complete, does it agree with itself, does it meet the requirement that applies, and can the answer be defended later. PharmaTrust is the machinery for asking those questions consistently.
What the foundation provides
These are shared, and they are the reason a second document type is an extension rather than a rewrite.
Verified extraction
A value is only passed on if it can be shown to come from the page and the position it claims, above a confidence floor. Reading and judging are separate, so neither can quietly corrupt the other.
A controlled source register
Every requirement the system may cite is registered with its version. A rule that rests on a retrieved requirement cannot even switch on until a qualified person has recorded the reviewer, the date, the confirmed source version and a named regression test.
Findings with a fixed shape
Requirement, evidence, outcome, reason, severity, score impact, reference, required action, applicability. The constructor refuses a finding that restates its verdict instead of giving a reason.
A record that reproduces
Engine, template, model, source versions and rule fingerprint are stored per run, so a report from a year ago still resolves to the exact basis it was made on.
Where the platform is going
Direction, not a catalogue. Nothing below is available, none of it can be bought or trialled, and no dates are attached. It is here so you can judge whether the foundation is being built for the problems you actually have.
CEP review
Structured review of Certificates of Suitability to the European Pharmacopoeia against the current monograph and annexes.
DMF review
Assessment of Drug Master File documentation for completeness and internal consistency before a filing or a supplier qualification.
GMP and broader GxP compliance
Document-level checks across manufacturing, laboratory and distribution practice records.
Supplier intelligence
A qualification picture built from the documents a supplier has already provided, tracked over time.
Medical-device documentation
Technical documentation and conformity evidence review for medical devices.
If one of these is the problem you need solved, say so: what people ask for is what gets built next. Get in touch.
Start with the product that exists
The COA Validator is available today, with five automated analyses a month at no cost.