This guide helps you navigate the source. Confirm the current document, effective status and scope before acting. The reading prompts below are PharmaEdges explanations, not quotations or inspection findings.
WHO good manufacturing practices ↗About this reference
Find WHO GMP reference documents and associated technical-report material. Includes navigation guidance and an official source link.
Reference materialReading prompts
Use these prompts alongside the linked official document. They are a starting point for your own assessment, not a complete checklist.
Choose the relevant scope
Start with the GMP topic relevant to your manufacturing activity.
Read the source in context
Record the document title, report or annex identifier and version you use.
Apply through your quality system
Assess applicability alongside local requirements and approved procedures.
Questions to consider
- Start with the GMP topic relevant to your manufacturing activity.
- Record the document title, report or annex identifier and version you use.
- Assess applicability alongside local requirements and approved procedures.
Document your assessment
Record the document identifier, version, applicable market and relevant scope. Route any necessary action through qualified personnel and your approved quality system. This guide does not determine batch release, filing decisions or compliance.