Visionary Medical Supplies has always been committed to making no compromises on quality. This is exemplified by many of our products carrying certifications such as US FDA 510(k) or the European Union CE Mark. But product quality is so much more than a strict adherence to standards and regulations; it is our guiding philosophy. This is why we practice Total Quality Management within our company, and have honed our internal processes in such a way that our products exceed the standard quality specifications at all stages of production.
OUR POLICY ON QUALITY
OUR QUALITY ASSURANCE SYSTEM
Our quality assurance team has developed a proven quality system for the manufacturing processes, beginning with the selection of raw materials, handling the manufacturing process, maintenance of the manufacturing area, sterility validation, packaging and labeling, validating equipments etc. This team also develops guidelines, imparts adequate training and ensures compliance to standards and regulatory requirements.
The raw materials used are sourced only from trusted suppliers who have a long, proven track record of the best quality materials.
This helps us establish the basis of quality in each of our products, right from the first stage of production.
BRINGING PRODUCTS TO MARKET
The quality assurance system that we have in place ensures that our products meet and often exceed the strict specifications and requirements put forth by the United States FDA and the European Union. Furthermore, all the new products introduced by Visionary Medical Supplies undergo strict studies on biocompatibility and pass clinical trials before being introduced in the commercial market.
FDA Establishment Registration
FDA Device Listings (Incl. 510K's)