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EU-MDR: Are You Ready? An Exclusive Three-Part FDAnews Webinar Series
The EU-MDR compliance clock is ticking. Your legacy products marketed in the EU are at serious risk unless you act now. Many devicemakers still aren’t ready. The transition is one complicated set of rules!
FDAnews has put together an exclusive three-part webinar series to help you get ready:
Find out why a PRRC is required in the first place and what is the PRRC duties and responsibilities
Determine whether the PRRC is over or under qualified or unable to fulfil their duties due to tasks overload
Get a sense of the relationship between the PRRC and the strategy set for regulatory compliance
Discover how the processes of a medical device manufacturer and other economic operators should be planned in order to fulfil the requirements for a PRRC
Critically evaluate whether your corporate structure is ready to ensure supervision and control of products to achieve EU regulatory compliance
Familiarize yourself with the importance of organizational design to ensure the various roles participating in compliance are understood and coordinated
How to prepare other related plans — the complaint management plan, the trend report plan and if applicable, the PMCF plan
How to determine the reports required for the PMS System
How to determine when to prepare a PMCF plan
Understand the content of the PMCF Evaluation Report
How to link PMS data and PMCF data to risk management
Ensure your EU-MDR readiness. Register today to join us for the exclusive three-part webinar series.
Three-Part Series Pricing
Webinar plus USB Audio Recording/Transcript Learn more
Best Value! You’ll have access to one log-in for the live 90-minute webinar for unlimited participants. You also receive all presentation materials and the opportunity to ask questions by phone and email, plus an USB audio recording and transcript for the entire session. Delivery is approximately two weeks after the session.
You get one log-in for the live 90-minute webinar for unlimited participants, presentation materials and the opportunity to ask questions by phone and email.
$646
24/7 Encore plus USB Audio Recording/Transcript Learn more
You'll have access to one log-in for an archived recording of the entire 90-minute webinar, including the Q&A period, for unlimited participants. You can log in any time of day or night. You'll also receive all presentation materials, plus an USB audio recording and transcript for the entire session. Delivery is approximately two weeks after the session.
You'll have access to one log-in for an archived recording of the entire 90-minute webinar, including the Q&A period, for unlimited participants. You can log in any time of day or night. You'll also receive all presentation materials.
You'll receive an USB audio recording and written transcript of the entire 90-minute webinar, including the Q&A period, and all presentation materials. Delivery is approximately two weeks after the session.
$646
Who Will Benefit
Quality Managers/Engineers
Risk Managers
Regulatory Affairs
Design Engineers
Supply Chain Managers
Production Managers/Engineers
Document Control Specialists
Marketing Managers
Clinical Managers
Clinical Evaluation Specialists
Export Compliance Managers
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