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Shaping the regulated quality of tomorrow.
Articles and analysis from our own work across GxP, pharma, quality management, GAMP and AI - what is changing in the regulated environment, what it means in practice, and what is happening inside our company.
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Data Management Audit of processes and computerized systems at an academic spinoff company
An academic spinoff company contracts QFINITY∞ to audit its data management processes for compliance with regulatory requirements. The audit also included the processes and documentation concerning the underlying computerized systems, including their validation status.
Validation of a laboratory process in a contract research organization
A manufacturer of high-performance ceramics for dentists and dental technicians planned to introduce a new ERP system and needed to take the new system’s 21 CFR Part 11 capability into account. QFINITY∞ also ran a workshop to work out the recommendations to consider for Part 11 in the new system.
Audit of the Quality Management Processes of a small/midsize CRO
A small-to-midsize CRO contracts QFINITY∞ to conduct an audit of the quality management system in order to identify opportunities for improvement. The audit comprised all the processes associated with the QM unit and its documentation.