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We have a dedicated quality assurance team at each production facility who examine the finished products before each shipments.

Our quality assurance procedures are carried out at various stages
of the production process, including incoming, in-process
and outgoing stages.

We establish quality assurance standards for the
individual customers and evaluate such standards on a continuous basis
with our customers.

To closely monitor our production processes, each of our product
groups has quality control team consisting of experienced technicians and
supervisors.

Our incoming quality control team and sourcing team work together
to inspect incoming raw material used in our medical products processes.

We require our raw material suppliers to establish and maintain
stringent quality assurance systems throughout their production processes
and be able to provide timely support in the event that incoming raw
material do not meet our quality standards.

Our raw material suppliers observe FDA, CE, or other relevant certification requirements depending on the intended market destination.

We perform quality checks at the ends of every stage of
production to ensure that the semi-finished medical products meet all
the relevant quality standards before we begin the next stage
of process.

We also implement comprehensive in-process quality control
checklists throughout the entire production process and record traceable
information to identify and address issues.

Finished medical products undergo further quality
assurance examination before they are shipped to our customers. In
addition, our quality assurance team located in our service centres
samples the incoming products to ensure that our quality meets or exceeds customer’s
expectations.

The ISO Certification is an international standard in
quality management device manufacturing, and it specifies
requirements for quality management systems where we need to
demonstrate our ability to provide medical devices and related services
that consistently meet customer requirement and regulatory requirement.