Quality and Standards

October 19, 2021 | Company News

MG Health’s Manufacturing Facility has been designed and is managed in line with GMP Guidelines. The company makes use of quality by design methodologies to ensure hygienic design, logical process flow and an HVAC system to ensure we have a controlled processing environment throughout. An Environmental Management System (EMS) is in place to monitor and notify if any temperature or humidity in the facility goes out-of-specification (OOS).
Cannabis Flower is manufactured as an Active Pharmaceutical Ingredient (API) and is dried, cured, trimmed and sized before packaging takes place for final destination. The processes are managed based on Regulatory Requirements in the country of destination. Specification Sheets and Certificates of Analysis (COAs) are submitted for approval by the Quality Unit of the Customer.

Final APIs undergo testing as per the German Monograph, with additional testing where required. The testing includes cannabinoid profiles, Loss on Drying (LOD), heavy metals, terpene profiles, pesticides as per Ph. Eur, mycotoxins, microbial contaminants as well as ash testing as and when required.
In line with GMP, batch traceability is maintained throughout all processes. This ensures that from harvest to the final packaged API your product’s quality is assured and maintained.