Quality is at the heart of our organisation. Patient safety is our number one priority, therefore we are committed to provide first class quality products and services.
The Healthcare industry is highly regulated and Unisurge International is fully compliant with all the required standards.
Unisurge International are accredited to ISO13485, the recognised quality standard relating to medical devices, and also the Medical Devices Directive 93/42/EEC. The processes and policies in place ensure continued compliance with the requirements of these standards.
Unisurge International Limited currently hold a Wholesale Dealers Licence allowing distribution of medicinal products and also a Manufacturing Licence allowing medicinal products to be included inside our procedure packs, both are controlled and regulated by the MHRA. Certificates of GMP Compliance are also held for each of the manufacturing sites.
|CE Mark Certificate Current – JAN 2016 – SEPT 2020||ISO 13485 CERTIFICATE – MARCH 2015 TO MARCH 2018||Manufacturer GMP Compliance 2014 – Newmarket||Manufacturers Licence (MIA Licence)|
|Own Brand Labelling EC Certificate – JAN 2011 – JAN 2016||Wholesale Dealers Licence (WDL Licence) – Current Version||Wholesale Distributor GDP Compliance 2014 – Newmarket||Wholesale Distributor GMP Compliance 2014 – Sawston|
|British Safety Council Member Certificate – Current Version||Apprenticeships in Partnership with Cambridge Regional College|