Digitalization, the use of informatics applications to transform the ways of working, can provide both regulatory compliance and business benefits to a lab.
This is the first in a series of three eBooks on planning and realizing a digital regulated laboratory, aimed mainly at Good Manufacturing Practice (GMP), but the principles outlined here can also be used for laboratories working to Good Laboratory Practice (GLP).
Download this eBook to explore topics including:
- What is Pharma 4.0?
- Data integrity within a pharmaceutical quality system
- A flexible analytical data life cycle
- Business drivers for digitalization
