Data Integrity: Advanced

Unlock the power of data integrity and compliance with “Advanced” category instrumentation. Ensure you comply with 21 CFR Part 11 regulations as well as GMP/cGMP and pharma-industry regulations.

The “Advanced” category ensures you fulfill the regulatory requirements of pharmaceutical and biotech laboratories at all categorys and streamlines analytical processes, data collection, processing, storage, and review.

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Audit trail mode

Electronic signature

Enhanced electronic signature

Data printout

Protected data storage

Restricted time and date setting

Data backup

Electronic data transfer

User management with fixed password rules

Individual user group management

Configurable password security

Looking for more features? Check out our other data integrity categories on our overview page here.

Compatible Products

Data Integrity, Security and Compliance in Regulated Industries.

Understand 21 CFR Part 11 requirements. Delve into detailed descriptions of individual features. Explore how measuring technology and pharmacopeia chapters relate.

Download the comprehensive e-book “Data Integrity, Security and Compliance in Regulated Industries.”

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