
At EMEDICS PHARMACEUTICALS LIMITED, quality is not just a department — it is the foundation of everything we do. Our Quality Management System (QMS) is designed to ensure that every product leaving our facility meets the highest standards of safety, efficacy, and quality.
We are committed to full compliance with World Health Organization Good Manufacturing Practices (WHO-GMP) and the regulatory requirements of the Tanzania Medicines and Medical Devices Authority (TMDA).

EMEDICS has established a comprehensive Quality Management System built on internationally
recognised standards and best practices in pharmaceutical manufacturing.

Comprehensive QA systems covering all stages of production, from raw material sourcing to finished product release, ensuring batch-to-batch consistency.

State-of-the-art QC laboratory equipped for raw material, in-process, and finished product testing including chemical, physical, and microbiological analysis.

Full compliance with WHO-GMP, TMDA regulations, and regional harmonisation standards including EAC, SADC, and AfCFTA requirements.
Our manufacturing facility has been designed from the ground up to comply with WHO-GMP standards. Every aspect of our operations, from facility design to personnel training, is aligned with international quality requirements to ensure patient safety and product efficacy.
Our facility is designed with HVAC systems, cleanroom classifications, and material flows that prevent cross-contamination and ensure product integrity throughout the manufacturing process.
All manufacturing and testing equipment undergoes rigorous installation, operational, and performance qualification (IQ/OQ/PQ) to ensure consistent and reliable operation.
All personnel receive comprehensive GMP training covering hygiene, documentation, standard operating procedures, and quality culture to maintain the highest standards of manufacturing practice.
GMP Compliance Target
Quality Control Tests
Regulatory Approvals Targeted
Acres of Facility
