Course offering number:0903-205
Course ID:
2092
ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
11-13 March 2009
Dublin, Ireland
Bea Salis; Consultant, QualASyst International
Bea Salis has over a 25 year career in Regulatory and
Quality Assurance for both drug and medical device
companies. After working more than 18 years with
various divisions for Baxter, she worked for startup new
medical technology companies to help bring exciting
products from the idea stage into clinical trials or
preparation for marketing. Ms. Salis also has been
instrumental in building startups into Wall Street traded
companies. She has lectured widely in the US and
abroad, and is now a full time consultant to the medical
device industry. Her specialty is implementing, and
compliance to regulatory and quality systems for both
the US and Europe. Ms. Salis is an ASQ Certified
Quality Engineer and a Certified Quality Auditor.
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