GxP
Good [x] Practice (GxP)
GxP is an umbrella term for regulatory "good practice" guidelines such as GMP (manufacturing) or GDP (distribution) in pharma and life sciences.
GxP: Not to be confused with
GxP is NOT a single standard. GxP is an umbrella term for different guidelines depending on the activity, for example GMP for manufacturing, GDP for distribution or GLP for laboratory practice, each with its own requirements for documentation and systems.
Switzerland’s medicines regulator Swissmedic defines GMP as the set of rules that ensures the quality of pharmaceutical manufacturing, including validated processes and complete documentation (Source 1). For ERP systems, GxP compliance means changes to quality-relevant data must be traceably logged, often with electronic signatures and an approval workflow.
This is central for the Pharma & Life Sciences industry, with touchpoints also in the Chemicals & Process Industry.
Related terms
Sources for GxP
- Swissmedic, "GMP – Good Manufacturing Practice" ↗