ISO 9001 certification —
we do the work. You sign off.
Custom procedures, internal audit before the external one, and we're there on audit day. 23+ years. Zero rejections.
- End-to-end support — A to Z
- Procedures tailored to your company
- Training for key employees
- Internal audit before the external one
- Structured path to certificate
- Works for companies of 5–10 employees too
200+ companies certified. Zero audit rejections since 2002.
Who It Fits
ISO 9001 is a universal standard. We specialize in adapting it to your specific case.
Any sector with a product or service, internal procedures, and customers who expect quality will get value from ISO 9001. Our experience spans four core industries.
Industry & Manufacturing
Plants, machining, packaging, food — a quality management system tailored to production lines and process control.
Engineering & Projects
Civil, mechanical, electrical engineering — a system built for project-based work and complex delivery schedules.
Services & Logistics
Shipping, warehousing, agencies — procedures that organize the supply chain and guarantee a consistent customer experience.
Hi-Tech & Software
R&D, cybersecurity, managed services — a QMS that fits startups, agile development, and enterprise customer requirements.
What You Get
ISO 9001 pays for itself — and upgrades your company along the way.
Access to tenders that were previously closed to you
Most government and large-enterprise tenders require ISO 9001 as a prerequisite. Without it, you simply can't bid. The moment you have it — an entire market opens up.
Reduction in repeat errors
When procedures are written down and people work from them, the same defect doesn't come back twice. In practice that means fewer returns, fewer complaints, and less time spent firefighting.
Growth in customer trust
An international certificate is a professional ID card. Big customers check it before signing a contract — and it leaves the competition behind.
Time to onboard new employees
Written procedures = fast onboarding. A new hire understands their role, how things are done, and why — without grilling ten different colleagues.
Likelihood you'll run on processes, not on people
A company that runs on procedures doesn't collapse when the lead operator goes on vacation. It may be the quietest benefit of ISO 9001 — but the most meaningful one.
No Marketing — Just Facts
What ISO 9001 IS — and what it ISN'T.
We don't sell certificates. We sell a process. So you know exactly what you're signing up for.
ISO 9001 IS…
A method for managing quality — a set of procedures, responsibilities and measurements.
A common language with customers worldwide — recognized in 170 countries.
A prerequisite for many tenders — both government and private.
A comprehensive process — not a shortcut.
A small cultural shift — but a real one.
ISO 9001 IS NOT…
Not a wall certificate — if you don't actually use the procedures, it was a waste.
Not a check on whether your product is good — it audits the system that produces it.
Not heavy bureaucracy — done right, it actually saves bureaucracy.
Not a product you can finish in a week — anyone who promises that is lying.
Not only for big companies — even 5 employees is enough.
How We Work
Six structured stops — from scoping to certificate in hand
Initial assessment
A short visit on site. We map what already exists, what's missing, and the gaps against the standard's requirements.
Tailored procedures
We write the procedures — built around your company. No generic templates. Procedures that actually work in your environment.
Key-employee training
A focused workshop for the quality lead and relevant staff — so the system keeps running long after we leave.
Internal audit
An internal pass before the external audit. We surface gaps, fix them, and make sure there are no surprises.
External audit support
We're at your side on audit day. Answering, explaining, documenting. You're never alone in front of the auditor.
Certificate + annual maintenance
Got the certificate? Great. Now we handle the periodic surveillance audit, recertification, and continuous improvement — no surprises.
Meet Shai Lis
We don't sell you a certificate. We build you a system that works.
Shai Lis has led LIS Quality since 2002. Over 200 companies have earned ISO 9001 certification with him — from 5-person startups to industrial plants of hundreds. His approach: never pile on procedures, never write for the wall. Only what you'll actually use — and use for real.
We don't leave the company once the certificate arrives. We leave once we've verified the system is alive.
What Our Clients Say
Without the professional guidance and support of Shai and the LIS team, we could not have met the standard's requirements. We gained immensely from his deep knowledge and extensive experience in work processes, especially in our facility.
To Shai and the dear team — after a challenging ISO 13485 audit day, I want to thank you for your professional approach to understanding our organization's unique needs, your creative thinking in finding solutions, and the specific tailored work methods that aren't visible on the surface.
FAQ
The questions company leaders ask us
How long does it take?
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It depends on company size and operational complexity. In a brief consultation we'll review your situation and agree on a realistic timeline.
Is it suitable for a small company (5–15 employees)?
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Absolutely. Most of our clients are exactly this size. Small companies actually see the biggest impact — because the procedures start working quickly and reshape day-to-day operations.
Will we have to change a lot in the company?
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Less than you'd think. We don't replace the way you work — we document it. If something already works well, we capture it. If it doesn't, we improve it together. No revolution required.
How much does it cost?
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It depends on company size and operational scope. One comprehensive proposal — no add-ons later. In a 15-minute consultation we can give you an accurate range.
What's the difference between ISO 9001 and ISO 13485?
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9001 is a universal quality management standard, suitable for any sector. 13485 is specific to medical devices — based on 9001, but with stricter regulatory and documentation requirements.
What happens in the years after?
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There's an annual surveillance audit and a full recertification every 3 years. We support those too — so you never have to start over.
Do we need a quality manager in the company?
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You need a quality lead — not necessarily full-time. In small companies it can be the owner or an existing VP who takes on the responsibility. We train them.
Other Standards
Need a more specific standard?
ISO 13485 Certification
The mandatory quality standard for medical devices — the foundation for every regulatory approval worldwide.
AMAR Registration
Medical device registration with the Medical Equipment Division — required for every sale in Israel.
Need a different track?
CE Marking, FDA, ISO 27001, AS9100 — we're a professional home for every certification.
Let's Get Started
15 minutes. One comprehensive quote — no add-ons, no surprises.
Leave your details and we'll send you one document promptly: a realistic timeline, the documents you'll need, and an accurate price range. No pressure, no “urgent proposal”.
Three fields. We'll come back with a professional assessment — not a high-pressure pitch.
No commitment. No mailing list. We reply within one business hour.