|
Since
2004 TRICOMED S.A. has held a certificate confirming that Quality
Assurance System conforms to the requirements of standard EN ISO
13485:2003 encompassing design, manufacturing and sales of medical
devices.
Quality
Assurance in our company encompasses the earliest planning phases in
every significant area which has tangible effect on product quality, its
safety and usefulness. As a
manufacturer of medical devices of all classes we ensure that the
assurance process is dynamic. The basic principle of Quality Assurance
is total and fundamental rule of company management consisting in
constant striving for result improvement by means of bringing to
perfection the customer service with simultaneous taking into
consideration the needs of all parties.
Our
mission is to improve the safety by utilization of biomedical
technologies in tests, manufacturing and providing access to innovative
medical devices which contribute to pain alleviation,
restore health and lengthen lifespan.
Along
with certificate EN ISO 13485:2003 the company obtained CE Mark
confirming that
manufactured medical devices conform to all requirements concerning EU
directives and that we have fulfilled all procedures of compliance
evaluation.
|
