GMP Medical Cannabis
Good Manufacturing Practice (GMP) is the definitive standard for manufacturing medical cannabis products intended for therapeutic use. It ensures that all products are consistently produced and controlled according to quality standards, which is crucial in the rapidly evolving cannabis industry.
What is GMP?
GMP is a systematic approach that governs the entire production process, from the starting materials to the final products. It encompasses all aspects of production, including:
- Consistent high quality;
- Suitability for intended use;
- Compliance with all applicable regulations.
Why do we need GMP for Medical Cannabis?
Implementing GMP is vital to ensure that cannabis medicines are safe and effective. The standards help to minimize risks associated with production that cannot be eliminated through testing alone. GMP requirements cover various aspects of manufacturing, including the following:
GMP ensures that:
- The production environment is controlled and sanitary;
- Staff are trained and maintain proper hygiene;
- Detailed, written procedures are followed for each manufacturing process;
- Documented evidence exists to demonstrate that proper procedures are consistently adhered to.
Medical Cannabis GxP: Good Practices for Medical Cannabis
- GAP: Good Agricultural Practice: Propagation and Cultivation
- GMP: Good Manufacturing Practice: Processing Herbal Product into Medicines
- GDP: Good Distribution Practice: Sales, Brokerage and Distribution
- GCP: Good Clinical Practice: Prescribing and Clinical Trials
- GLP: Good Laboratory Practice: Clinical Testing and Analytic Testing (Also covered by ISO)
- Rhizo Sciences Quality Statement for Medical Cannabis
