OAK & NINE
HomeBy industry/for-regulated-processes
For pharma, clinical, medical-device & regulated finance

“We think we do it that way” doesn’t pass an audit.

In a controlled world, what you assert you have to prove. Hold your procedures under version control with sign-off and periodic review, and ground every fact in its source, so an inspection is a formality rather than a scramble.

QualityClinicalOperationsComplianceOne connected baseEvery procedure, signed and dated
What changes

Built around how your world works.

01
Audit-ready by default

Every change tracked and signed, nothing deleted, a full history: the trail auditors expect, kept without extra effort.

02
Periodic review, enforced

Every procedure carries its next-review date; you learn what’s due before an inspector does.

03
Provenance on every fact

Only human-confirmed knowledge counts toward your controlled picture, and each fact has a source behind it.

04
Traceable across the chain

Follow a batch or a study from supplier to release across functions: the connections auditors ask for, already mapped.

Proof
100%
Every controlled fact, traceable to source.

Provenance, sign-off, and an immutable review history.

Capability statement only, not a certification claim. Wording subject to legal approval.

See it on your own business.

A short walkthrough on your own business, no preparation needed.