Welford’s business is to form a partnering relationship with the healthcare institutions for the advancement of better health care by supplying quality medical devices using our resources of design, manufacturing and logistics. We form our values, design our process and make our decisions in line with such partnership principle.
We work with the best material suppliers, and we design the devices using the best available know-how. We manufacture our devices by implementing the highest quality standards. We actively engage in promoting the best clinical practices by exchanging expertise and ideas with the healthcare providers. By following close partnering principle, Welford delivers medical devices that are of excellent quality and consistently meet if not exceed the expectations of our customers.
As a result of the relentless commitment of our management, Welford obtains the ISO 13485 certification from TUV SUD of Munich Germany. Our products carrying CE marking are certified meeting the standards of the European Community Medical Design Directive MDD 93/42/EEC, and hence are approved to be freely sold in the European markets.
To ensure the safety of our devices, Welford places great emphasis on the regulatory compliance. Products testing and regulatory documents are prepared and compiled to fulfill the standards of not only the European markets but also the competent authorities in other nations.
Our packaging process is challenged using the stringent US ASTM methods, and is further qualified by accelerated aging tests and real time tests in compliance with the ISO standards. By this, we verify and guarantee the sterility and the shelf life of our devices.
Quality assurance is the key element in Welford’s manufacturing process. Our quality checking activities and suppliers qualification and monitoring programs are designed and performed fulfilling the requirements of available ISO standards that are relevant for each device in our range.