Assuring the integrity of records when generating and maintaining them is essential to the development and production of high-quality, safe, and effective drugs.

This white paper reviews the US and European regulations, and details how records generated by the Palltronic Flowstar V integrity test instrument meets the requirements. The scope of the paper includes:

The scope of the paper includes:

Access control demands
The structure and classification of the electronic records generated by the instrument
ALCOA plus principles
Audit trail management

Download the white paper today to see how we designed the Palltronic Flowstar V instrument for the highest assurance of data integrity.

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