Sonora Medical Systems, a leading supplier of after market products, services and test equipment to the medical imaging market, announces that Ms. Julie Morris, BSME, Manager of Quality and Regulatory Affairs at Sonora, has fulfilled all the requirements of the Regulatory Affairs Certification Board administered by the Regulatory Affairs Professional Society, and has become Regulatory Affairs Certified (RAC). The RAC examinations (US, EU and CAN) are knowledge-based exams addressing laws, regulations, policies and guidelines affecting regulated healthcare products, including medical devices, pharmaceuticals, biologics and biotechnology in their respective regions. The RAC is awarded to individuals who perform well on a comprehensive
examination testing knowledge of FDA and related US laws, regulations, policies and guidelines, with an emphasis on medical devices, biologics and pharmaceuticals. The RAC also identifies individuals who are committed to excellence, pursuit of knowledge and career development.

"The RAC certification for Morris is another example of Sonora leading the after-market medical device industry in the pursuit of excellence in both quality and regulatory adherence. RAC certification is a public recognition of professional achievement-both within and outside the profession," said G. Wayne Moore, President and CEO of Sonora Medical Systems.

In addition to designing and manufacturing industry unique ultrasound and endoscopy test devices and repairing thousands of diagnostic ultrasound probes per year, Sonora Medical Systems is the largest and fastest growing ultrasound and MRI depot-level repair company in the United States and its operations are certified to ISO9001/13485 quality standards. Sonora Medical recently celebrated its 11-year anniversary in business.

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