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Recalls & Vigilance-When to Report Complaints
This webinar will acquaint one with the lessons learned from over 30 years of adverse events and complaints.
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John Chapman
Regulatory Affairs Professional,This webinar will acquaint one with the lessons learned from over 30 years of adverse events and complaints.
View DetailsThis presentation will help you to understand ISO 13485 and implement a successful quality management system, comparing it to ISO 9001 and FDA & European Union requirements.
View DetailsImproper complaint handling can result is serious regulatory problems as well as hitting the bottom line.
View DetailsISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards.
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