About

Ensuring Stringent Postmarket Monitoring through Thorough Complaint Monitoring Strategies,
Streamlined Data Management and a Comprehensive Understanding of Global Quality Expectations
2
Days
9
Speakers
1
Sponsor
15
Sessions
13. - 14. February, 2024 | Chicago, IL, USA

8th Annual Medical Device Postmarket Surveillance Professional Engagement Course

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Speakers

Queenita Fernandes
Queenita Fernandes
Sr. Medical Safety Manager MEDTRONIC
Camilla Borrini
Camilla Borrini
Associate Director QARA PMO ZIMMER BIOMET
Seth Mailhot
Seth Mailhot
Partner HUSCH BLACKWELL
Susana Hidalgo
Susana Hidalgo
Manager Post-Market Surveillance ESTABLISHMENT LABS
Barry Sands
Barry Sands
President and Founder RQMIS
Marta Carnielli
Marta Carnielli
Head of Certification IVD, TÜV SÜD Product Services GmbH TÜV SÜD
Diptha Ramaswamy
Diptha Ramaswamy
Medical Writing and Clinical Post Market Surveillance Senior Manager ZIMMER BIOMET
Stephanie Berger
Stephanie Berger
PMS EU MDR Lead PHILIPS
Leah Featherstone
Leah Featherstone
Sr Quality Systems Program Manager, Data Intelligence MEDTRONIC

Program

9:00 AM - 9:20 AM

ZOOM SIGN-ON & VIRTUAL PROGRAM WELCOME

Main Stage

9:20 AM - 9:30 AM

Chairperson's Opening Remarks

Main Stage

9:30 AM - 10:15 AM

LEGAL PERSPECTIVE: EXAMINATION AND CLARIFICATION OF NOTABLE FDA GUIDANCES

Main Stage

Seth Mailhot

10:15 AM - 11:00 AM

STREAMLINING OPERATIONAL READINESS TO COMPLY WITH EU MDR

Main Stage

Camilla Borrini

11:00 AM - 11:30 AM

VIRTUAL NETWORKING & COFFEE BREAK

Main Stage

11:30 AM - 12:15 PM

PRACTICAL APPROACHES TO POSTMARKET PMCF DEVELOPMENT IN COMPLIANCE WITH EU MDR

Main Stage

Diptha Ramaswamy

12:15 PM - 1:00 PM

CASE STUDY: ROBUST PRODUCT PERFORMANCE MONITORING & TRENDING

Main Stage

Leah Featherstone

1:00 PM - 1:15 PM

Module One Conclusion

Main Stage

Contact information

Event date:
13. February - 14. February, 2024
Event location:
Chicago, IL, USA
Organizer:
Q1 Productions [email protected]
Contact organizer

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