Join us for our October Webinar - "Auditing Through the Medical Device Development Cycle: From Start-Up to Commercial" presented by Mary Duffy.
Startup companies in the medical device industry are often small affairs with basic quality management systems. As the product progresses through the design and development stages from prototyping to production the QMS also has to grow and mature. In parallel, the audit program needs to reflect these changes in the development cycle to ensure that the QMS is sufficiently mature at the time the commercial product launch. In this session, we will look at the how your tailor the auditing approach through the development cycle.
Bio: Mary Duffy is the Senior Director of Compliance and Quality Improvement at Kardium Inc., a medical device manufacturer in greater Vancouver, BC, Canada. She has worked in various roles in quality control, quality assurance and compliance in the biotech and medical device industries for over 30 years. She received a doctorate in analytical toxicology from the University of Saskatchewan in Saskatoon. Mary is a senior ASQ member and holds four certifications. She has been an active member of the ASQ Vancouver SLC since 2012.
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Please register through the link below:
https://asq.webex.com/weblink/register/ra599a7bb0b0c38af4673a1e535268016