General Questions

We provide industrial pharmaceutical consulting, GMP-compliant facility design and construction, regulatory advisory, quality systems support, and market access services.

 
Yes. We support projects from feasibility and planning through design, construction, compliance, commissioning, and operational launch.
We design and deliver cGMP-compliant manufacturing plants, laboratories, warehouses, and cleanrooms with optimized workflows, safety, and scalability.
We align projects with local and international regulations, including NAFDAC, WHO, GMP, ICH and ISO standards, ensuring audit readiness and sustained compliance.
Yes. We provide market access support, including regulatory pathways, product registration, and market entry strategy development.

Other Questions

We optimize manufacturing processes, facility layouts, quality systems, and supply chains to reduce costs and improve productivity.
Yes. We support QMS implementation, SOP development, validation, and continuous improvement initiatives.
Our services support pharmaceutical manufacturers, investors, startups, CMOs, and healthcare enterprises.
Yes. We provide hands-on project management, contractor coordination, commissioning, and handover support.