This guide explores how regulated laboratories can achieve strong data integrity by digitalizing key processes ...

Digital transformation has been a consistent drumbeat in the industry for the past few years and is a core piece of many enterprises’ business strategies. Successful digital transformation is the ...

The term "data integrity" can mean different things to different people, but the most difficult and pervasive problem facing organizations these days is the semantic integrity of the data. As ...

In this interview, AZoM talks to Simon Taylor from Mettler Toledo’s Titration product group about data integrity in titration and why it is important to do so for laboratories, production lines or ...

Randy Barrett is a freelance writer and editor based in Washington, D.C. A large part of his portfolio career includes teaching banjo and fiddle as well as performing professionally. An organization ...

The pharmaceutical industry’s approach to data integrity has been historically manual, leveraging physical documentation and potentially unreliable paper-based ...

The present world of digital transformation, streamlining workflows, enhancing operational efficiencies, and eliminating paper demands connected workflows with fully integrated systems and equipment.

Our Food, Drug & Device/FDA Group breaks down the new Food and Drug Administration guidance on data integrity for current good manufacturing practices (CGMPs) and what it means for the drug industry.

Kathleen Hurley is the founder of Sage Inc., a tech company that offers SMB businesses infrastructure solutions and next-gen technology. As data becomes everything to everybody, it’s crucial to ...

Earlier yesterday, FDA published the final guidance “Data Integrity and Compliance With Drug CGMP: Questions and Answers,” which updates April 2016 draft guidance that covers the design, operation, ...