From data integrity regulations to Pharma 4.0

Read a scientific instrument vendor’s perspective on the impact of the changes that one of their largest customer industries will undergo and what influence this will have on the evolution of software required to operate analytical instrumentation and the underlying handling of data.

The industry white paper highlights topics highlight:
* Challenges in Drug Production – Batch production versus Continuous Manufacturing
* Thermo Scientific™ Chromeleon™ 7.3 Chromatography CDS Audit Trail Review framework
* Demonstrating Data Integrity; Data Integrity as an enforcement tool to improve drug quality
* and more!

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From data integrity regulations to Pharma 4.0

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