ISO
13485: 2003 for Medical Devices
Medical device manufacturers are looking beyond ISO 9001: 2000
for their quality systems. Formal certification of a QMS, specifically
for medical devices, to ISO 13485: 2003 proves advantageous,
and in many cases essential, for medical companies which export
their products to the global market. Learn what it takes to
develop a system that meets these industry-specific requirements.
Seminar Fee: $795
All meals, excluding dinner, are included.
Each participant will receive a comprehensive
manual and a Certificate of Completion at the close of the
seminar.
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