As a leading pharma exporter, our foundation is built on uncompromising quality. We adhere strictly to globally recognized regulatory frameworks to ensure every product manufactured at Daffohils Laboratories is safe, effective, and compliant, no matter its final destination.
Our manufacturing facilities operate under the stringent guidelines of the World Health Organization’s Good Manufacturing Practices (WHO-GMP), affirming our commitment to producing pharmaceutical products of the highest international standards. This, combined with our ISO certification, ensures systematic quality management across all processes.
WHO-GMP Certified: Our entire manufacturing process, from facility design to packaging, meets global benchmarks for quality.
ISO 9001:2015 Standards: Implementation of a robust Quality Management System (QMS) ensuring consistency.
Audited and Approved: We regularly undergo successful audits by global regulatory bodies and our international clients.
We leverage hi-tech technology (as mentioned in your old content) and modern, validated machinery to achieve good productivity with low manufacturing costs, without sacrificing quality. Our commitment to cutting-edge infrastructure allows for the efficient and scalable production of our diverse product range.
Dedicated zones for Oral Solids (Tablets/Capsules) and Liquids (Syrups/Suspensions).
HVAC Systems maintaining ISO 8 cleanroom environment and controlled pressure differentials.
Automated manufacturing and packaging lines for precision and contamination control.