ISO 9001 Service

Documentation an auditor can follow — and your team will actually use.

ISO 9001:2015 requires specific documented information and retained records. Our partners build the set you need, in your language, mapped to the processes you actually run.

Illustrative sample

Document register

QMS scopeReady
Quality policyReview
Document control procedureReady
Supplier evaluationGap

Why buyers choose this

Documentation support should make the quality system easier to run, easier to sample, and easier to keep current.

Only what the standard requires

Build the documented information ISO 9001 calls for, not a binder nobody opens.

Written for your processes

Procedures that describe how your team works, so the evidence matches reality.

Records that survive sampling

Auditors sample records. Structure them so retrieval takes minutes, not days.

Control that holds

Version control, approval, and review cycles that keep the system current after certification.

From scattered files to a controlled system

The work starts with what already exists, then turns it into documented information your teams can own.

01

Where you are

Documents exist in five places, three versions, and one person's head.

02

What we do

Map required documented information to your processes, then draft, structure, and control it.

03

Where you land

A controlled document set and a records index you can hand to an auditor on day one.

What changes once the system is controlled

The required set, not a template dump

ISO 9001:2015 requires the QMS scope, a quality policy, and quality objectives to be maintained as documented information, plus retained records across areas like competence, calibration, supplier evaluation, nonconformity, internal audit, and management review. Partners build that set against your processes.

  • QMS scope, policy, and measurable objectives
  • Process documentation and work instructions where they add control
  • Retained-records structure by process

Control that outlives the project

Document control is where many first-time systems struggle during surveillance. Partners set up approval, revision, and review so the set stays current.

  • Approval and revision workflow
  • Review cadence with named owners
  • Obsolete-document handling
What's included

A documentation workstream with handover built in

  • Documentation gap review against clauses 4–10
  • QMS scope statement and justified exclusions
  • Quality policy drafted with leadership
  • Measurable quality objectives and monitoring plan
  • Process documentation and work instructions
  • Document control procedure and register
  • Records index mapped to required retained information
  • Handover training for document owners

Deliverable snapshot

The finished package should make ownership, status, and record location obvious before anyone starts sampling.

Illustrative sample

Document Clause link Owner Rev Status
QMS Scope4.3Quality1.0Ready
Quality Policy5.2Leadership0.9In review
Quality Objectives6.2Leadership0.8In review
Document Control Procedure7.5Quality1.0Ready
Competence Records7.2HR1.0Ready
Supplier Evaluation8.4.1Purchasing0.7In review
Nonconformity & Corrective Action10.2Quality0.9In review
Internal Audit Programme9.2.2Quality0.8In review

Compare documentation paths

Every Andvio partner clears a vetting bar and commits to a 48-hour response SLA on questions.

Capability Andvio partners Off-the-shelf template kit Generalist consultancy Build it in-house
Documentation mapped to your real processes●○◐●
Only the documented information the standard requires●○◐◐
Document control set up, not just documents delivered●○◐◐
Records index tied to retained-information requirements●○◐◐
Owner training and handover●○◐○
Independent of any certification body●●◐●
Fixed scope●●◐◐
Responsive partners (48h SLA on questions)●○◐○
● Full support ◐ Partial support ○ Limited support
How much documentation does ISO 9001 actually require?

Less than most template kits sell. ISO 9001:2015 requires certain documented information to be maintained, including the QMS scope, quality policy, and quality objectives, plus retained documented information (records) across areas such as competence, monitoring and measuring resources, supplier evaluation, nonconformity and corrective action, internal audit, and management review. Beyond that, you document what your organization needs to control its processes. See ISO's ISO 9001 overview.

Will you write our procedures for us?

Partners draft with your process owners rather than around them. Documentation that no one recognizes fails at the audit interview, not at the document review.

Does this include the internal audit?

No — that's a separate service. See Internal Audit & Certification Support.

Can this be done remotely?

Most of it, yes. Tell us during matching whether you need on-site work and for which sites, and we'll route accordingly.

We already have an AS9100 manual. Is that enough?

AS9100 is built on ISO 9001 with added aerospace requirements, so much of your existing documentation is likely reusable. Partners start by reviewing what you have rather than replacing it.

What does it cost?

Pricing depends on the number of processes, sites, and existing documents in scope. Matched partners quote against your actual scope; Andvio's matching is free and requires no retainer.

Turn a folder of documents into a controlled quality system

Get matched with a partner who can turn your current procedures, records, and owner knowledge into documentation your team can maintain.

Free matchNo retainerSpecialists respond within 48 hours