Industries·Pharma and life sciences
GMP without the paper chase.
Deviations, CAPA, change control and training kept complete, traceable and signed.
- Frameworks
- GMP, ISO 9001
- Teams
- Quality, Continuous improvement, Operations
Conflicts withWI-3.2Redlinerev. 7 draftedApproved14 people to briefWhere the paperwork piles up
Four places it piles up in pharma and life sciences.
01
Deviations that wait days for a report
02
CAPAs that close without proof they worked
03
Change control across hundreds of SOPs
04
Training records that lag behind revisions
One event, handled
From the first signal to the last approval.
A deviation is reported on the line, by voice.
The report is drafted with the batch history and the change that preceded it.
The CAPA is assigned and the SOP revision drafted for the quality unit.
−52%All the evidence
defects with digital instructions instead of paper
Source · Letmathe & Rößler, Journal of Operations Management, 2022For your teams
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