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.
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.