Glossary
GxP
What is GxP?
GxPÂ in the pharmaceutical industry refers to a set of good practice guidelines and regulations that ensure the quality, safety, and efficacy of pharmaceutical products throughout their lifecycle.
The “GxP” acronym stands for G – Good, x – Variables, P – Practices
The key aspects of GxP in pharmaceuticals include:
- Establishing quality systems and processes
- Ensuring product quality, safety, and efficacy
- Maintaining detailed documentation and records
What are the key features of GxP in pharma?
The key features of GxP (Good “x” Practice) in the pharmaceutical industry are:
- Regulatory Compliance: Compliance with GxP guidelines is mandatory for pharmaceutical companies to obtain and maintain approvals for manufacturing, distributing, and marketing their products.
- Quality Management: GxP principles focus on maintaining robust quality systems and processes throughout the pharmaceutical supply chain.
- Integrity: GxP regulations prioritize patient safety by ensuring pharmaceutical products are developed, manufactured, and distributed under strict quality control measures.
- Traceability: GxP requires comprehensive documentation and record-keeping to enable effective traceability of pharmaceutical products and processes.
