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Document Review

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ISO 9001 Document Review

Catch QMS Problems Before You Implement Them

Document Review Service

Have a lead auditor review your fully customized 9001Simplified Quality Management Manual before you roll it out. We find missing requirements, unclear or conflicting controls, and unnecessary complexity – then show you exactly what to correct.

Find Compliance Gaps

Catch Unclear or Unnecessary Controls

Know Exactly What to Correct

USD 1,440

Money Back Guarantee

Ratings and Reviews

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4.7

51 ratings

Reviewer Rating 5 Stars
84%
Reviewer Rating 4 Stars
0%
Reviewer Rating 3 Stars
16%
Reviewer Rating 2 Stars
0%
Reviewer Rating 1 Star
0%

Why Choose the Document Review?

Your manual is easiest to fix before your team starts using it. Get an experienced outside check while changes are still quick and easy to make.

Catch Gaps Before Implementation:  Find missing or incorrectly applied ISO 9001 requirements before they become embedded in everyday work.

Make the QMS Easier to Use:  Identify unclear instructions, duplicate controls, contradictions and unnecessary complexity before your team has to work with them.

Know What to Fix:  Receive specific findings and recommendations – not a generic checklist or a simple pass/fail verdict.

We thought we had customized the manual perfectly, but the review caught three issues where we had screwed up. Luckily, we hadn't started implementing yet.

Marc Fulbright  /  Keystone LLC

Keystone corrected the issues before implementation, completed the QMS, and later achieved certification.

How it Works

Finish your customization, send us the manual, and get a detailed expert review before implementation.

1.  Finish Your Customization

Complete your Quality Management Manual so it reflects how you intend the QMS to work. The review is most valuable before those documented controls are rolled out.

2.  Submit Your Manual

Upload your fully customized 9001Simplified Quality Management Manual using the instructions provided after purchase. You have up to 6 months to submit it.

3.  Lead Auditor Review

A lead auditor reviews the manual line by line against ISO 9001 requirements, looking for missing requirements, unclear or conflicting controls, unnecessary complexity, and places where the documentation may not work well in practice.

4.  Receive Your Findings

Within 7 days, you receive a detailed 20–30 page report with clear findings and specific recommendations so you know exactly what to correct before implementation.

A good document review should catch two kinds of problems: what could cause an audit finding, and what could make the QMS harder to use than it needs to be.

Simon Keller  /  Senior Consultant & Lead Author  /  9001Simplified

Meet Our Consultants

Andrew O'Reilly

Andrew O'Reilly

IRCA-certified Lead Auditor and ASQ-certified Six Sigma Black Belt with more than 25 years of experience in quality management, process improvement, project management and change management.

Andrew has helped clients successfully implement more than 100 quality management systems and has conducted well over 100 internal audits across multiple industries. That breadth of experience helps him quickly identify missing requirements, unnecessary complexity and documentation that does not accurately reflect how the business operates, while recommending practical corrections that strengthen both compliance and performance. more

Colin Gray

Colin Gray

Distinguished consultant and IRCA-certified Lead Auditor with more than 30 years of experience helping hundreds of companies across a wide range of industries.

Colin's strategic approach focuses on streamlined, effective processes that provide strong organizational control while driving continuous improvement and added value. His broad experience with ISO 9001, industry-specific standards and other management systems makes him particularly effective at identifying gaps, inconsistencies and unnecessary bureaucracy in complex QMS documentation. more

Robin Bathurst

Robin Bathurst

Lead Auditor and consultant with more than 20 years of specialized experience in medical testing, medical devices and manufacturing.

Robin's background in advanced process controls, consulting, training and auditing gives her particular strength when reviewing documentation for technical or highly regulated processes. She can assess whether controls are clearly defined, appropriately documented and robust enough for the risks and operational requirements involved. more

Simon Keller

Simon Keller

Lead Author and consultant with more than 25 years of experience in education and ISO 9001 quality management.

Simon is one of the lead architects behind our implementation methodology, ready-to-configure QMS documentation and training system. His specialty is translating complex ISO 9001 requirements into clear, practical documentation, making him especially effective at identifying where documents are unclear, overly complicated or disconnected from the way employees actually work. more

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Included
Line-by-line review of your customized 9001Simplified Quality Management Manual + detailed 20–30 page findings report.

Turnaround
Report delivered within 7 days of receiving your completed manual.

Prerequisites
Fully customized 9001Simplified ISO 9001 Quality Management Manual (available separately or in our Toolkit).

Clients We've Helped

Aeroprobe Link Solutions INC FM First Majestic Tri-Tec Manufacturing Tesla US Department of Defense Peublo Community College M&B Machine INC Faxitron US Army NEO Consult Rand Peter Lacke Paints Phillips 66 Sensical INC Matandy Siemens Energy TDK

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