ETHRA Pharmaceuticals designs and operates its Addis Ababa manufacturing facility in alignment with World Health Organization Good Manufacturing Practice (WHO GMP) principles.
Facility Design
Controlled environments, clear personnel and material flows, and dedicated production zones minimize cross-contamination risk across dosage forms.
Documentation and Traceability
Batch manufacturing records, change control, and deviation management ensure every product release is supported by complete documentation.
Regulatory Readiness
Our systems support customer audits, regulatory inspections, and continuous improvement — building trust with partners and patients alike.