At DANMIL, quality is built into every step of our process, from the selection of certified raw materials to the final integrity testing of our filtration solutions. Our manufacturing facility in Greve, Denmark, is cGMP validated and operates to the highest international standards. We comply with stringent global regulations, including FDA CFR Title 21, EU Regulation No. 1935/2004, and USP Class VI.

Every product is produced in-house for full control over quality and traceability. Materials and finished products undergo rigorous testing, including cytotoxicity growth inhibition, physicochemical testing (USP 27) chapter <661>, FDA LAL Guideline (3) and USP, and reverse mutation testing. All results are validated by an independent, cGMP-certified laboratory, ensuring reliable performance in the most demanding applications.

Our commitment to excellence goes hand-in-hand with sustainability. We continually invest in advanced manufacturing technologies, improve processes, and adopt responsible practices that reduce environmental impact while maintaining the highest quality standards.