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

21 Jul 2016

Webinar

Key Topics

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

Who should Attend

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

Past Events

FDA's Emerging Signals Guidance: Reporting Medical Device Safety Warnings 2016 - 21 Jul 2016, Webinar (60780)

FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings 2026

Important

Please, check "FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings" official website for possible changes, before making any traveling arrangements

Event Categories

Business: E-Business, Human Resources (HR), Internal Audit & Compliance, Quality assurance

Government & Global Issues: Law & Regulations

Health & Medicine: Healthcare, Medical device, Pharma

Industry: Food & Beverages

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