MFT Consult specializes in pharmaceutical manufacturing, biopharma, clinical testing, and regulatory compliance—particularly in Africa and the Middle East.

Yes. We offer end-to-end support for facility conceptual design, commissioning, and validation for production plants, clinical labs, and bioequivalence centers.

Absolutely. Our team provides full regulatory support, including dossier preparation, supplier qualification, and compliance with WHO, FDA, and EMA standards.

We tailor GMP-compliant QMS frameworks including SOPs, CAPA processes, audits, and continuous improvement programs suited to each facility's unique operations.

We primarily serve pharmaceutical companies across Africa and the Middle East, with a deep understanding of both international and local regulatory requirements.

Yes. We support technology transfer, scale-up activities, and help optimize manufacturing workflows from R&D to commercial production.

Our cross-disciplinary expertise, regional focus, and commitment to regulatory excellence position us as a reliable partner for pharma startups and expansions.

Yes. We provide continuous consultancy and technical support to ensure sustained compliance, performance improvements, and readiness for future audits or expansions.