Data Integrity Resource Center
The sheer volume of information on data integrity can be overwhelming. To make it easier for you to find relevant information, we have compiled a list of resources in one place.
Moving to the Cloud: Trends, Opportunities, Considerations, Next Steps
Data Integrity in Pharma QC Labs: What You Need to Know
Demystifying Software Validation: Learn What Software Validation Means for You and Your Lab
Support for Title 21 CFR Part 11 and Annex 11 Compliance: OpenLab CDS
Support for Title 21 CFR Part 11 and Annex 11 Compliance: OpenLab Server and OpenLab ECM XT
Support for Title 21 CFR Part 11 and Annex 11 Compliance: Agilent OpenLab ECM
Support for Title 21 CFR Part 11 and Annex 11 compliance: Agilent MassHunter for LC/MS
Support for Title 21 CFR Part 11 Compliance: Agilent MassHunter for GC/MS
Support for Title 21 CFR Part 11 and Annex 11 compliance: Agilent OpenLab EZChrom with OpenLab ECM
May require registration
Is Chromatography Ready for the Cloud, Part 1 & 2
Data Integrity Tips for Regulated Laboratories, Part 1
Data Integrity Tips for Regulated Laboratories, Part 2
Data Integrity in Regulated Laboratories, Part 1
Data Integrity in Regulated Laboratories, Part 2
Data Integrity in Regulated Laboratories, Part 3
Data Integrity in the GxP Chromatography Laboratory, Part 1
Data Integrity in the GxP Chromatography Laboratory, Part 2
May require registration
Current Perspectives for CGxP Compliance: A Conversation with Monica Cahilly, 3-Part Podcast Series
Windows 7 End of Support – How to Plan for and Execute the Migration, 3-Part Podcast Series
Combined Top-Down/Bottom-Up Approach to Data Integrity, 3-Part Podcast Series
May require registration
Five Essentials for Surviving Your Next Laboratory Inspection: A Quality Control Example
A Practical Approach to Building an Electronic Laboratory
Addressing Data Integrity Gaps: Does Your Lab Have a Strategy?
Addressing the Paradigm Shift in Regulatory Inspections
Moving to the Cloud: Key Considerations
Controlling Chromatographic Integration to Ensure Data Integrity
Demystifying Software Validation
Part 1: Five Essentials for Surviving Your Next Laboratory Inspection: A Quality Control Example
Part 2: Five Essentials for Surviving Your Next Laboratory Inspection: A Quality Control Example
Addressing Data Integrity Gaps: Does Your Lab Have a Strategy?
Moving to the Cloud: Key Considerations
Addressing the Paradigm Shift in Regulatory Inspections
Controlling Chromatographic Integration to Ensure Data Integrity
Ensure Data Integrity in Your Analytical Lab: Inspection Checklist
Welcome to the Brave New World of CSV
5 Tips for Avoiding Data Integrity Issues in Chromatographic Integration
Calculating & Reporting Results: 4 Tips for Preserving Data Integrity
5 Ways to Maximize the Effectiveness of Second-Person Reviews
Stopping Data Manipulation Tricks in their Tracks During Instrument Setup and CDS Data Acquisition
6 Pointers for Passing Your Next Data Integrity Inspection
Computerized Systems in Drug Establishments
A Framework for Innovative Pharmaceutical Development, Manufacturing, and Quality Assurance
Guidance for Industry Part 11, Electronic Records; Electronic Signatures - Scope and Application
MHRA GxP Data Integrity Definitions and Guidance for Industry
Data Integrity and Compliance with cGMP Guidance for Industry
General Principles of Software Validation; Final Guidance for Industry and FDA Staff