Quality Systems in the Medical Device Industry
This training is intended to inform company management all other levels within the organization the additional requirements above and beyond ISO 9000 which are required by business operating in the medical device field. In addition to the voluntary requirements established by ISO 13485 there are regulatory requirements dictated by the FDA, Health Canada and the European Union that must be complied with to allow for the development, manufacturing, sale and marketing of medical devices.
This training is complementary to our Quality Management System development services which can be found here.
Course Time: 4 -8 Hours depending on the companies requirements
Course Fee: Quotation available on request.
To request a quote for training please e-mail us at email@example.com.