Vigor is committed to providing the highest level of quality in both traditional and modern manufacturing processes.
Consistent quality of supply is the ‘key’ to success for any company operating in the medical devices sector. To help support this commitment, Vigor Healthcare has invested heavily across its Chinese manufacturing operation and following this investment,
In 2012 the Quality Management System was certified according to Medical devices directive – Quality Management Systems ISO-13485: 2003.
In 2019 the Quality Management System was updated and certified
according to the new standard ISO-13485: 2016.
Vigor is committed to providing the highest level of quality both in traditional and modern manufacturing processes.
Any material vendors approved as being able to achieve the consistently high standards demanded by Vigor additionally are required to comply with ALL ISO/BS standards (preferably 13485), adhere to clear environmental policies and comply with international human rights agreements and conduct business in an ethical manner.