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!

Premium Access

To access this content please enter your details in the fields below.

Name

Company

Telephone

Email

Country

I confirm that my contact details can be forwarded to the author and/or the author's company of each White Paper I visit during this time. I understand that my contact details will not be made available to any other third party. To view our full privacy policy please click here.

From data integrity regulations to Pharma 4.0

Premium Access

Editor's picks

Fault-tolerant quantum computing 'will solve exciting science problems'