NF EN ISO 13485 is an internationally recognized standard for ensuring the regulatory compliance of medical devices.
GMED certifies that the quality management system developed by SOPAC MEDICAL for the manufacturing and sale of droppers complies with the requirements of the international standard NF EN ISO 13485:2016.
This certification reflects SOPAC MEDICAL's strong commitment to continuous improvement and is a guarantee of confidence in packaging that is both safe and effective.
GMED certifies that the SOPAC MEDICAL production quality assurance system complies with the requirements of Annex V point 3 of Directive 93/42/EEC for obtaining and maintaining the sterile state of medical devices.
SOPAC MEDICAL is one of the winning companies selected by the Île-de-France region for its development projects over the next three years. This support, labeled "Powered by Paris Region," truly demonstrates the relevance of its industrial investments and its interest in the Île-de-France region.
Ethical charter “A responsible relationship with our stakeholders”: As part of its responsible and sustainable development policy, SOPAC MEDICAL has defined an ethical charter to be respected.
In order to carry out our measurements, we can rely on our supplier PCE instruments France whose responsiveness is highly appreciated and allows us to obtain highly precise control measurements. www.pce-instruments.com