How to comply with data integrity | Agilent

Scientists in the lab

Data Integrity: Download our 75 Point Checklist

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Data Integrity Checklist- find the problems in your GMP lab

What would an auditor find in your lab:

QC analysts sharing the same user name and password?

Electronic raw data that has been deleted?

Unauthorized employees able to generate or access data?

The audit trail has been switched off?

Use our 75 point data integrity checklist to fix the problems in your GMP lab before an auditor finds them.
Pharma forum: Data integrity and compliance

This expert presentation and discussion forum focuses on data integrity and compliance, particularly in QA/QC, development, and manufacturing. Experts highlight why technology companies need to put the customer at the heart of innovation to develop solutions, not just products. They examine how different technologies can offer benefits for regulatory compliance, with examples of how instrumentation, data integrity, and compliance have been combined to provide effective solutions.

Watch on-demand discussion now
Take a look at the data integrity controls offered by Agilent OpenLab and the Cary 3500 UV-Vis

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Useful literature

If you'd like to explore the Agilent Cary 3500 UV-Vis spectrophotometer and Agilent OpenLab combination, here's literature with the details:
To determine if the Agilent Cary 3500 UV-Vis can meet your analytical needs, here are some examples of what it can do:
- Application note:Measuring Total Sulfite in Sucrose According to the USP43- NF38-6076 Method
- Technical overview: Photometric Accuracy and Linear Dynamic Range of the Agilent Cary 3500 UV-Vis Spectrophotometer
- Whitepaper: Support for Title 21 CFR Part 11 and Annex 11 Compliance: Agilent Cary UV Workstation Software for Cary 3500
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Cary 3500 features

Software

Cary 3500 UV-Vis

Improve ALCOA+ data integrity

Meeting FDA 21 CFR Part 11 requirements

Comply with global pharmacopeia

Remove variables with simultaneous measurements

Reduce risk with simpler protocols

Amplify confidence with the Cary 3500

Improve ALCOA+ data integrity

Meeting FDA 21 CFR Part 11 requirements

Comply with global pharmacopeia

Remove variables with simultaneous measurements

Reduce risk with simpler protocols

Amplify confidence with the Cary 3500

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