Tag: FDA 21 CFR Part 11

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What is IQ/OQ/PQ? Stages of Equipment and Systems Validation

The validation of equipment, systems, and processes is essential to ensure that they function correctly, safely, and according to specifications. The IQ/OQ/PQ model is an established methodology in the pharmaceutical, cosmetic, food, medical, and electronic industries, especially those following standards such as GMP, ISO 13485, FDA 21 CFR Part 11,

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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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