Enterprise-wide Quality & Integrated Management System

Enterprise-wide Quality & Integrated Management System EwQIMS is a web-based Enterprise Quality Management Software for all your business quality operation

Omnex Systems, LLC is headquartered in Ann Arbor, Michigan and provides Software solutions to improve the quality of businesses worldwide and help achieve certification requirements. Founded in 1984 by Chad Kymal, we are on track to be one of the world's largest quality consulting, software and training providers. Our staff of experienced quality consultants, engineers and programmers provide "one

-stop shopping" programs to all client companies. The experience of our senior management adds special value to top management activities.

18 applications. 32 global sites. One product risk challenge.How do you bring real-time risk visibility into a complex p...
09/10/2026

18 applications. 32 global sites. One product risk challenge.

How do you bring real-time risk visibility into a complex product development environment?

This case study reveals how a leading semiconductor company adopted a “Shift-Left” approach using FMEA and real-time data integration to identify product risks earlier, reduce scrap and rework, and unify risk data across its global operations.

See what changed — and how.

👉 Read the full case study. https://hubs.li/Q04x6_S80

Real-time shop floor data can do more than track performance. It can help manufacturers identify patterns, anticipate po...
09/04/2026

Real-time shop floor data can do more than track performance. It can help manufacturers identify patterns, anticipate potential quality issues and act before they impact production.

With predictive insights, teams can make faster decisions, strengthen process control and stay ahead of defects.


Turn your shop floor data into smarter decisions.

Request a demo https://hubs.li/Q04wLpnH0

AIAG-VDA FMEA is more powerful—but also more complex.Since the release of the AIAG-VDA FMEA Handbook, many organizations...
08/28/2026

AIAG-VDA FMEA is more powerful—but also more complex.

Since the release of the AIAG-VDA FMEA Handbook, many organizations have struggled with creating consistent, efficient, and effective FMEAs.
But what if technology could make the process smarter?

In this recorded webinar, Mary Rowzee and Sarah Hathaway explore advances in applying the AIAG-VDA FMEA methodology and how modern FMEA software can help teams:
• Reduce errors and improve consistency with Inheritance
• Reuse proven knowledge through Design and Process Libraries
• Transition more seamlessly between AIAG 4th Edition and AIAG-VDA
• Explore the role of AI and Machine Learning in FMEA development
• Build a more efficient and standardized approach to risk analysis

▶ Watch the webinar recording on YouTube:
https://hubs.li/Q04vFWN70

Your 8D is closed. But why does the problem keep coming back?Closing a corrective action is not the finish line.True pro...
08/27/2026

Your 8D is closed. But why does the problem keep coming back?
Closing a corrective action is not the finish line.

True problem-solving requires teams to move beyond closure and focus on:
Root Cause → Action → Verification → Prevention

But can AI help quality teams make this process faster, more structured, and more effective?

Join Mike Popenas and Antony John as they explore how AI can support stronger problem-solving, improve 8D and CAPA effectiveness, and help turn recurring issues into opportunities for prevention.

📅 October 15, 2026
⏰ 11:00 AM EST

Join us for this exclusive webinar — at no cost.
REGISTER NOW - https://hubs.li/Q04vz3zc0

PPAP documentation was becoming a major bottleneck. For a global semiconductor manufacturer, preparing PPAP documentatio...
08/25/2026

PPAP documentation was becoming a major bottleneck.

For a global semiconductor manufacturer, preparing PPAP documentation meant pulling data from SAP, SharePoint, network drives, and several business applications.

The process was fragmented, heavily manual, and required 1.5 days per analyst, while customer-submission-ready documentation could take 3–4 workdays.
How did they bring that down to just 1.5–2 hours?

Discover the approach behind the transformation.

Read the case study → https://hubs.li/Q04v9S6p0

Managing controlled documents across ISO, IATF, FDA, aerospace, medical device, cybersecurity, and other compliance requ...
08/21/2026

Managing controlled documents across ISO, IATF, FDA, aerospace, medical device, cybersecurity, and other compliance requirements doesn’t have to mean managing separate systems.

Document Pro helps organizations centralize document control, manage revisions and approvals, maintain compliance, and keep the right information accessible when it matters.

From ISO 9001 and IATF 16949 to AS9145, FDA CFR 21 Part 11, ISO 13485, and more—bring your document management processes into one controlled system.

Explore Document Pro and simplify document control across your standards.

🔗 https://hubs.li/Q04tQsNv0

Modern NPD involves a wide range of areas such as software, hardware, electronics, global project teams and above all, a...
08/19/2026

Modern NPD involves a wide range of areas such as software, hardware, electronics, global project teams and above all, a massive amount of product data. But does “digitizing” these areas actually make NPD less complex?

Correct NPD digitalization means linking up planning, requirements, risk management, traceability and product data - NOT simply digitalizing individual processes.

Are you digitalizing NPD or just “digitizing” the chaos?

Find out more in our whitepaper
https://hubs.li/Q04tvMHt0

From Static FMEAs to Intelligent Risk SystemsYour FMEA may be complete. But is it complete enough to uncover the risks y...
08/14/2026

From Static FMEAs to Intelligent Risk Systems
Your FMEA may be complete. But is it complete enough to uncover the risks you haven’t seen yet?

Traditional DFMEA and PFMEA can become static spreadsheets—manually created, inconsistently structured, and disconnected from production data.

In this webinar, “Agentic AI for FMEA Generation, Validation, and Continuous Improvement,” Chad Kymal and Antony John explore how Agentic AI can transform FMEA into a dynamic, continuously learning risk engine.

You’ll discover how AI can:
🔹 Generate DFMEA, PFMEA, and Control Plans from product and process inputs
🔹 Validate logic across DFMEA → PFMEA → Control Plan
🔹 Detect missing risk linkages across the Digital Thread
🔹 Recommend stronger prevention and detection controls
🔹 Use shop-floor and SPC data to continuously improve risk models

The goal isn’t simply to create FMEAs faster.
It’s to identify risks earlier, strengthen traceability, and build a closed-loop quality system.

▶️ Watch the webinar to see how Agentic AI can reshape the future of FMEA and quality engineering.
https://hubs.li/Q04t29pR0

Every Audit. One Intelligent Platform. Audits shouldn't be scattered across spreadsheets, emails, and paperwork. With Au...
08/06/2026

Every Audit. One Intelligent Platform.

Audits shouldn't be scattered across spreadsheets, emails, and paperwork.

With Audit Pro, you can manage all audit types, schedule audits, conduct online and mobile audits, streamline CAR responses, and support Layered Process Audits (LPA)—all in one centralized platform.

Ready to simplify your audit process? Explore Audit Pro. - https://hubs.li/Q04s5_Y-0

We're growing our YouTube community and we'd love to have you with us. Subscribe to our channel and stay connected wit...
08/04/2026

We're growing our YouTube community and we'd love to have you with us.

Subscribe to our channel and stay connected with everything happening at EQMS AI, from product updates to event highlights and more.
👉 Subscribe here - https://hubs.li/Q04rPt5Q0 👈

Address

315 E. Eisenhower Parkway, Suite 300
Ann Arbor, MI
48108

Telephone

(734) 761-4940

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