What we do
QMSiQ provides client relationship management, certification planning, and audit delivery as a member practice of Equal Assurance. Our approach combines experienced auditors, responsive communication, and personalized service with the governance and certification framework of the Equal Assurance network.
Why choose QMSiQ
Experienced auditors. Clear communication. Personal service. QMSiQ delivers a responsive, client-focused certification experience backed by the Equal Assurance network. Our goal is to make the certification process straightforward, professional, and easier to manage from application through ongoing surveillance.

“Price is what you pay, value is what you get” – Warren Buffett
Highlights
- Extensive auditing experience with ISO 9001, the AS9100 series, and other management system standards across manufacturing and technical industries.
- Focused on management system certification activities, including initial certification, surveillance, recertification, certification transfers, and related audit support.
- Experienced quality auditors with strong industry knowledge, technical competence, and practical understanding of complex operational environments.
Services Offered

Initial Certification
For organizations pursuing Quality Management System certification for the first time, we coordinate the certification process with you from application review through Stage 1 and Stage 2 audit activities.
Certifiable program schemes available:
ISO9001 – Quality Management
ISO13485 – Medical Devices
Verifiable program schemes available:
AS9100 – Aerospace Quality Management
AS9110 – Aerospace Quality Management (Aviation Maintenance)
AS9120 – Aerospace Quality Management (ASD Distribution)

Certification Transfers
Organizations already certified by another accredited certification body may be eligible to transfer their certification. We will review the existing certification and applicable records to determine transfer eligibility and next steps.
Transferable program schemes available:
ISO9001 – Quality Management
ISO13485 – Medical Devices

Ongoing Certification
For current QMSiQ clients, we coordinate surveillance, recertification, scope changes, special audits, and other activities needed to maintain an established certification account.
If you have had a significant change in your organization which could impact your certification, please contact your Client Manager to discuss next steps.
Your Certification Journey
01
Inquiry & Application
Tell us about your organization, sites, activities, certification scope, and objectives.
02
Application Review
We review your information to confirm scope, certification requirements, resource needs, impartiality, and audit duration.
03
Proposal & Acceptance
You receive a proposal defining the certification scope, audit activities, fees, timing assumptions, and applicable terms.
04
Stage 1 Audit
The initial audit evaluates your management system, organization, site conditions, and readiness for the certification audit.
05
Stage 2 Certification Audit
The audit team evaluates implementation and effectiveness of your management system against the applicable certification requirements.
06
Certification & Ongoing Surveillance
Following successful technical review and certification decision by Equal Assurance Partner, certification is issued and maintained through scheduled surveillance and recertification activities.
Industries and Sectors

Precision Manufacturing
Pivotal to economic growth, driving innovation, and creating employment opportunities. We service machine shops and precision manufacturers demonstrate consistent processes, reliable quality, and effective control of production, inspection, and customer requirements.

Aerospace & Defense
Supporting suppliers and service providers that need disciplined quality management, strong process control, and greater confidence throughout demanding Aerospace, Space and Defense customers and supply-chain environments.

Distribution & Logistics
From the procurement of raw materials to the final delivery of products to consumers, we support distributors, warehouses, and logistics providers who require effective control of order fulfillment, supplier management, product handling, traceability, and customer service.

Electronics & Cable Assembly
Working with electronics, cable, and wire-harness organizations where process control, workmanship, inspection, traceability, and supplier management are critical to product quality.

Chemical Manufacturing
Characterized by complex processes, stringent safety and environmental regulations, and a strong emphasis on research and development, we support clients to stay relevant in both statutory and regulatory requirements.

Metal Fabrication
Essential for the manufacturing of metal components and products used in various industries such as construction and automotive, we ensure our clients maintain quality, precision, and innovation to meet the demands of diverse applications and markets.
Expertise
Our team has years of industry experience across several global sectors and disciplines
- 15+ years working with large Aerospace and Defense OEM’s
- 15+ years experience in Manufacturing and Production
- 15+ years experience in Quality Management Systems
- 15+ years conducting 1st, 2nd and 3rd Party Audits
- Authenticated Aerospace Experience Auditors
- ISO 9001 Certified Lead Auditors
- ASQ Certified Quality Auditors
- ASQ Certified Quality Engineers

Experienced auditors focused on your certification experience.
Need Assistance?
Frequently Asked
Questions
Who issues my certification?
Certification is issued through the Equal Assurance Partner. QMSiQ manages the client relationship, audit planning, and audit delivery, while the certification decision and certificate issuance remain under the Partner’s authority.
What is the difference between Stage 1 and Stage 2?
Stage 1 reviews your management system and readiness for certification. Stage 2 evaluates whether your management system is fully implemented and effective against the applicable standard.
How long does certification take?
Timing depends on your organization’s readiness, size, complexity, and scheduling needs. The timeline is coordinated with you after application review, and certification generally must be completed within 12 months of proposal acceptance.
How many audit days will I need?
Audit duration depends on factors such as employee count, number of sites, processes, shifts, complexity, and certification scope. QMSiQ determines the required audit time after reviewing your application.
Can I transfer an existing certificate?
Yes. Existing accredited certifications may be eligible for transfer. QMSiQ will review your current certificate, recent audit history, open findings, and certification status to determine eligibility.
What happens after certification?
Certification is maintained through periodic surveillance audits, followed by recertification at the end of the 3-year certification cycle.

Still have questions?
Can’t find the answer you’re looking for? Let’s schedule a meeting to discuss your needs.

