Why ClearVue
Built for the Way Manufacturers Actually Work
Most ISO compliance tools were built for enterprise pharma or cobbled together from generic project software. ClearVue was designed from the ground up for ISO-obligated manufacturers with 25–500 employees.
Sound familiar?
Most customers come to us from one of these three situations.
You manage documents in SharePoint or shared drives
There is no approval workflow, no version control, and no way to prove an employee ever read the current revision. Every audit starts with a scramble.
ClearVue replaces that with a controlled document lifecycle — approvals, versioning, acknowledgement tracking — built in from day one.
You were quoted $50K+ for an enterprise QMS
The platforms built for medical device or pharma manufacturers are priced and sized for procurement teams, not quality managers at 100-person shops.
ClearVue is priced for SMB manufacturers — no per-user fees, no six-month implementation, no features you will never use.
You have an upcoming audit and gaps you cannot close fast enough
Your last internal audit found findings you tracked in a spreadsheet. Some got fixed. Some did not. You cannot prove which is which.
ClearVue Audit Manager and CAPA give you a closed-loop system — finding to corrective action to verified fix, all documented.
What makes ClearVue different
Built clause-by-clause for ISO 9001
Every module maps to a specific ISO clause. When an auditor asks for evidence of Clause 9.2 conformance, you open Audit Manager and show them — not a folder of PDFs.
Workflow governance is not an add-on
Approvals, escalations, and audit trails are built into every record type. Document control, CAPAs, audit findings — nothing moves without a controlled process.
Priced for 25–500 person manufacturers
Flat annual pricing. No per-user fees that punish growth. No enterprise contracts that require legal review. Sized for the way SMB manufacturers actually buy software.
On the infrastructure your IT team already trusts
Azure-native hosting, SSO-ready, role-based access control. No new vendor risk to justify to IT. Deployable in your own Azure tenant if required.
Start where your gaps are biggest
Buy one module or the full ISO 9001 Pack. Most customers start with Document Control and Audit Manager — the two areas auditors probe first — and expand from there.
Evidence on demand
Every approval, acknowledgement, and corrective action is timestamped and retained. When your certification body asks for documented information, you produce it in minutes.
Built by people who have been in your shoes
ClearVue was founded by a team with backgrounds in manufacturing operations, quality management, and enterprise software. We have sat through certification audits, managed document control in spreadsheets, and tracked CAPAs in email threads. We built the tool we wished existed.
Meet the team →See it for yourself
A 30-minute demo scoped to your current compliance gaps. No sales pressure, no generic slide deck.
Request a Demo