Pharmaceutical Instrument Qualification Demo

Pharmaceutical and biopharmaceutical manufacturing is tightly regulated, to ensure product safety. Manufacturers seek to operate in a fully qualified environment, with validated processes.

For business reasons, time- and cost-efficient qualification and validation protocols must be balanced against the intensive, in-depth, comprehensive, and of course fully traceable efforts involved. The current trend is to focus on single-test approaches, employing tests and evaluations that are as safe, effective, and efficient as possible.

To support your compliance and traceability needs, Anton Paar offers more than 80 instrument-specific qualification packages as well as qualified installation support. This qualification service reduces the work required by your in-house personnel to make your new instrument ready for routine operation by 60 % - 70 %.

The packages go significantly beyond simple installation: they’re prepared individually for every system, and include all required documents for complying with relevant regulations.