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Agenda

Timely Implementation Strategies for Complying with New Regulations and Guidelines

April 10, 2018
  • London, United Kingdom

Agenda

Want more agenda details? Download the brochure.

TUESDAY, 10 APRIL 2018

7:30

Conference Registration and Refreshments

8:30

Chairperson’s Welcome and Opening Remarks

Philippa Montgomerie
Senior Director Legal and Compliance
EMEA, Medtronic

Take a Deep Dive into
the Medical Devices Regulation

8:45

Unearthing a Roadmap for the MDR Eudamed

Philippa Montgomerie
Senior Director, Legal and Compliance
EMEA, Medtronic

9:30

EU MDR and the Medical Device Single Audit Program — Playing Together!

Howard Broadbridge
Practice Manager
NSF Health Sciences

10:15

Networking and Refreshment Break

10:45

Implement MDR Guidelines While Submitting to Notified Bodies

Paul Sim
KS Medical Devices Knowledge Manager
BSI Group

11:30

Evaluate the Most Important Necessities for Keeping Medical Devices on the Market Under the MDR

Ronald Boumans
Senior Global Regulatory Consultant
EMERGO, a UL company

12:15

Luncheon

13:30

Examine the Impact of GDPR on the Medical Device Industry

Elisabethann Wright
Partner
Hogan Lovells

14:15

US Enforcement Landscape

John Oroho
Executive Vice President & Chief Strategy Officer
Porzio Life Sciences, LLC

Brian Sharkey
Vice President
Porzio Life Sciences, LLC

15:00

Networking and Refreshment Break

Key Changes That will Affect MedTech Europe Code of Ethical Business Practices in 2018 and Onward

15:30

Best Practices for supporting Third Party Medical Education according to the New MedTech Europe Code of Ethical Business Practices

Mathias P. Gubler
Associate Director, Compliance Office
Zimmer Biomet EMEA

16:15

Hot Topics Roundtable Review the most popular topics surrounding the MDR & MTE Code

Howard Broadbridge
Practice Manager
NSF Health Sciences

Ronald Boumans
Senior Global Regulatory Consultant
EMERGO, a UL company

Mathias P. Gubler
Associate Director, Compliance Office
Zimmer Biomet EMEA

17:00

Close of Conference

Networking, Wine and Cheese Reception immediately following the final session on day one

Agenda

Want more agenda details? Download the brochure.
Want more agenda details? Download the brochure.

TUESDAY, 10 APRIL 2018

7:30

Conference Registration and Refreshments

8:30

Chairperson’s Welcome and Opening Remarks

Philippa Montgomerie
Senior Director Legal and Compliance
EMEA, Medtronic

Take a Deep Dive into
the Medical Devices Regulation

8:45

Unearthing a Roadmap for the MDR Eudamed

Philippa Montgomerie
Senior Director, Legal and Compliance
EMEA, Medtronic

9:30

EU MDR and the Medical Device Single Audit Program — Playing Together!

Howard Broadbridge
Practice Manager
NSF Health Sciences

10:15

Networking and Refreshment Break

10:45

Implement MDR Guidelines While Submitting to Notified Bodies

Paul Sim
KS Medical Devices Knowledge Manager
BSI Group

11:30

Evaluate the Most Important Necessities for Keeping Medical Devices on the Market Under the MDR

Ronald Boumans
Senior Global Regulatory Consultant
EMERGO, a UL company

12:15

Luncheon

13:30

Examine the Impact of GDPR on the Medical Device Industry

Elisabethann Wright
Partner
Hogan Lovells

14:15

US Enforcement Landscape

John Oroho
Executive Vice President & Chief Strategy Officer
Porzio Life Sciences, LLC

Brian Sharkey
Vice President
Porzio Life Sciences, LLC

15:00

Networking and Refreshment Break

Key Changes That will Affect MedTech Europe Code of Ethical Business Practices in 2018 and Onward

15:30

Best Practices for supporting Third Party Medical Education according to the New MedTech Europe Code of Ethical Business Practices

Mathias P. Gubler
Associate Director, Compliance Office
Zimmer Biomet EMEA

16:15

Hot Topics Roundtable Review the most popular topics surrounding the MDR & MTE Code

Howard Broadbridge
Practice Manager
NSF Health Sciences

Ronald Boumans
Senior Global Regulatory Consultant
EMERGO, a UL company

Mathias P. Gubler
Associate Director, Compliance Office
Zimmer Biomet EMEA

17:00

Close of Conference

Networking, Wine and Cheese Reception immediately following the final session on day one