SURU manufactures CE marked medical devices in strict compliance with International manufacturing and regulatory requirements, all products are produced and packaged within state-of-the-art clean rooms and controlled environments in compliance with EU medical directives and Good Manufacturing Practice (cGMP).

Production facilities have been constructed and maintained in accordance with the GMP requirements for cleanliness. Plant operations are maintained for high quality standards by qualified and experienced technical personnel and trained workforce. All employees are trained regularly for personal and clean room hygiene. Utmost attention is provided to minimize contamination from external sources.

As a part of quality assurance, we carry stringent quality testing at each & every stage of manufacturing processes; intensive in-process quality control for components assembly  & packaging help us provide quality products.