OpenText Quality Management

A complete solution for life sciences organisations to ensure quality regulatory compliance in their products and services

Download our quality management paper and find out how OpenText allow you to integrate CAPA, audit, training and regulated document management into a single quality management solution, capture, track and manage key quality issues and initiatives, including observations, complaints, adverse events, deviations, non-conformances and audit findings, comply with the FDA's 21 CFR Part 11 regulation for electronic records and electronic signatures and provide various reports related to audits, CAPA, Training and more.

 

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