FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings 2016

FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings 2016 is a webinar that covers topics such as:

• Unique Device Identifier
• Guidance on Emerging Signals
• Case for Quality
• Electronic MDR reporting
• Moving from Reactive to Predictive Quality Management

FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings 2016 is intended for attendees from:

• Quality and Compliance Specialists
• Quality Systems Specialists
• Quality/Compliance managers or directors for Medical Device companies
• Internal Auditors and Managers
• General Managers wanting to strategize and prepare for future changes