2-day In-person Seminar I October 26th & 27th, 2017
Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system.
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President, Ombu Enterprises
San Diego, CA
DoubleTree by Hilton, San Diego Downtown
ENROLL NOW **Please note the registration will be closed 2 days (48 Hours) prior to the date of the seminar.
Course "Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach" is brought to you by the Global Compliance Panel and has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.