Daniel Davis, PhD

Daniel Davis, PhD, is a global GMP compliance specialist with Lonza Group Ltd.

Articles

James L. Brooks;Kurt In Albon;Daniel Davis, PhD

July 2nd 2015

Heightened regulatory scrutiny of data integrity highlights the need for comprehensive procedural reviews and strategies for managing mission-critical information.

Latest Updated Articles

Published: October 11th 2024 | Updated: October 18th 2024

Buy, Sell, Hold: Cell and Gene Therapy - Part 1

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Published: September 10th 2024 | Updated: September 18th 2024

CPHI Milan Announces 2024 CPHI Pharma Award Finalists

Published: October 28th 2024 | Updated: November 22nd 2024

Discovery to Commercialization: The Right Partnerships are Key to Streamlined Drug Development

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Published: November 6th 2024 | Updated: November 22nd 2024

Automate Aseptic Filling: Closing the System at Full Modularity

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Published: November 5th 2024 | Updated: November 22nd 2024

Untethered Data: Unifying and Contextualizing Drug Discovery Data

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Published: November 8th 2024 | Updated: November 22nd 2024

Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification

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