Ideagen Quality Control

Automated quality inspections for manufacturing excellence

Ideagen Quality Control automates quality inspections and documentation processes specifically for aerospace and defense, automotive, and medical device manufacturing firms.

The system streamlines inspection workflows while ensuring compliance with industry-specific quality standards and regulatory requirements. Built for highly regulated manufacturing environments, it provides comprehensive quality documentation, inspection management, and compliance reporting capabilities that support continuous improvement initiatives and regulatory adherence across complex manufacturing operations.

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Additional reading

KRA: Optimizing audit processes for ISO 9001:2015 compliance

KRA improve critical business processes and their transition to ISO9001:2015

Silcoms: Streamlining product management

Founded in 1939, Silcoms, a specialized manufacturing supplier of aerospace parts, chains, and components, faced challenges in managing processes like the ballooning of drawings and conducting test plans due to a lack of a centralized system. With Ideagen, Silcoms significantly improved their quality control processes, leading to greater efficiency and strengthened customer confidence.

Tecomet reduces production part approval process by 80%

Tecomet, a leader in manufacturing high-precision medical devices and aerospace components, aimed to modernize its New Product Introduction (NPI) and Production Part Approval Process (PPAP) to enhance efficiency and reduce approval times.

How to identify a suitable supplier who will adhere to AS13100

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How does AS13100 relate to me in aerospace and defense?

If you’re producing engines or their components in the aerospace and defense industry, it’s highly likely that you’ll need to comply with AS13100. Click to find out how.

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When your best expert retires: How AI preserves irreplaceable EHS & quality knowledge

59% of workers over 55 plan to retire within 5 years. Discover how embedded AI captures irreplaceable expertise before your best experts walk out the door.

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Why speed now determines who wins contracts in regulated manufacturing

Document quality during proposal development creates competitive advantage. Control the complete document lifecycle, from collaborative drafting through approval to archive.

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Why clinical trial success rates are declining and what document collaboration has to do with it

Document quality during trial development creates risks that QMS alone can't prevent. Control the document lifecycle, from first draft to final archive.

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AI-enabled systems and CSA: future-proofing your GxP compliance

Discover how FDA's CSA guidance enables compliant AI validation in GxP environments, reducing timelines by up to 95% while ensuring patient safety.

CSA vs CSV: Why risk-based thinking is transforming life sciences validation

Discover how the shift from CSV to CSA is transforming validation in life sciences. Learn how to accelerate innovation while ensuring compliance.