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High QA Manufacturing Quality And Supplier Quality Software

Helping You Meet AS9100, AS13100, IATF 16949, ISO 13485 and Other Industry Quality Standards

High QA software is a powerful manufacturing Quality Management Solution (QMS) to comply with industry quality standards and customer requirements. It helps you meet aerospace (AS9100, AS13100), automotive (IATF 16949), medical (ISO 13485) and other industry standards.

High QA develops an integrated manufacturing quality software platform that enables manufacturers and customers within their own facility and throughout their supply chain to automate the manufacturing quality process from quoting to delivery for parts that are on-time, on-budget and on-quality.

The database-driven software provides manufacturing quality and supplier quality management tools to ballooning drawings, create control plans and generate the required documents for part submission warrants and FAI, PPAP, PFMEA SPC and other quality documents.

High QA Production Quality Planning (High QA PQP) is a powerful manufacturing Quality Management Solution (QMS) to fulfill APQP and PPAP process requirements and helps you meet aerospace (AS9100, AS13100), automotive (IATF 16949), medical (ISO 13485), and other industry standards.

The comprehensive software solution helps you comply with manufacturing quality regulations, standards and requirements in automotive, medical, aerospace, defense, and other industries.

Choose Your Quality Standard

AS13100

AS9100

IATF 16949

ISO 13485

AS13100, AS9100

Quality Standard for Aerospace, Defense

What is AS13100?

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What is AS9100?

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How High QA Helps

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IATF 16949

Quality Standard for Automotive, Transportation

What is IATF 16949?

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How High QA Helps

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ISO 14385

Quality Standard for Medical Devices

What is ISO 13485?

ISO 13485 is the international standard that specifies requirements for a quality management system (QMS) where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services. Requirements of ISO 13485 are specific to organizations providing medical devices, regardless of the type or size, and can be used by any organization involved in one or more stage(s) of the life-cycle of a medical device.

How High QA Helps

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Comply with Industry Standards and Meet Customer Requirements and Expectations

See how you can simplify your manufacturing quality process, comply with your industry standards and meet your customers' requirements.
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