Tag: ISO 9001

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🏭 What is IATF 16949 and its importance for testing and production?

The IATF 16949 is one of the most important quality standards for the global automotive industry. Published by the International Automotive Task Force (IATF), it integrates the requirements of ISO 9001 with specific demands of the automotive sector, focusing on continuous improvement, defect prevention, and reduction of variations and waste.

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What is ISO 9001 and its impact on testing processes?

ISO 9001 is an international standard that sets criteria for a Quality Management System (QMS). Applicable to any type of organization, its focus is to ensure that processes are well-defined, controlled, and oriented towards continuous improvement and customer satisfaction. In the context of test engineering, production control, and test benches,

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What is R&R – Repeatability and Reproducibility?

R&R is the acronym for Repeatability and Reproducibility, two fundamental components of the study of measurement system capability. This type of study, also known as Gage R&R, evaluates whether a measurement system (manual or automated) is accurate, reliable, and consistent, regardless of who performs it or when the measurement is

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How TestStand, LabVIEW, and MES help meet standards and certifications in Brazil

Automated testing solutions like NI TestStand, LabVIEW, and integrated MES systems not only optimize test bench performance — they are key tools for ensuring compliance with technical standards and certifications required by national and international markets, especially in regulated sectors such as automotive, medical, electronic, and industrial. Automating is more

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What are Standard Operating Procedures (SOP)?

The Standard Operating Procedures (SOP) or Standard Operating Procedures (SOP) are formal documents that clearly, objectively, and sequentially describe how to perform a technical or operational task in a safe, effective, and traceable manner. They are essential for standardizing industrial routines, ensuring consistent quality, facilitating training, and meeting regulatory requirements

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What is CAPA?

CAPA (from the English Corrective and Preventive Action) is a structured process aimed at identifying, correcting, and preventing the recurrence of problems or non-conformities in quality, production, or testing systems. CAPA is part of systems like ISO 9001, IATF 16949, FDA 21 CFR and other industrial standards, being essential to