Audit and consulting in automated systems quality
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Pharmaceutical industryValience has a long-standing practical experience in validation and
qualification of automated systems for the pharmaceutical industry, according to the United States regulations (GMP,
21CFR11) as well as european requirements (Annex 11). |
Information technologyValience 's know-how regarding software engineering processes, software development quality and databases design allows your company
to deploy all critical information systems, timely, easily and efficiently. |
Medical devicesValience supports your effort during the setup of the quality system and
the preparation of your medical devices regulatory files, according to the standards ISO/IEC 60601-1-4, ISO 13485 and
ISO 14971. |
