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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

Create a Framework for the Medical Devices Regulation (MDR)

Josephine Tolley
Regulatory Affairs
Johnson & Johnson

9:30

Review the Do’s and Don’ts of Transitioning into the New Medical Devices Regulation (MDR)

Robert Steele
Executive Vice President Quality Assurance, Regulatory and Clinical Affairs
Convatec

10:15

Networking and Refreshment Break

10:45

Evaluate the New Responsibilities of Stakeholders in the Supply Chain

Hilde Viroux
Director EURMEA RA, MD & Vision Care
Alcon

11:30

Implement MDR Guidelines While Submitting to Notified Bodies

Paul Sim
KS Medical Devices Knowledge Manager
BSI Group

12:15

Networking Luncheon

13:30

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

14:15

Examine the Impact of GDPR on the Medical Device Industry

Elisabethann Wright
Partner
Hogan Lovells

15:00

Networking and Refreshment Break

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

15:30

The First Major Change of MTE Code —
Best Practices for Supporting Third Party Medical Education according to the new MedTech Europe Code of Ethical Business Practices

Dr. Heidi K. Jauch
Vice President Compliance Officer EMEA
Zimmer Biomet EMEA

16:15

The Second Major Change of MTE Code —
The Transparency Disclosure Requirement

Suzanne Durdevic
Senior Director, General Counsel Europe EMEA
Boston Scientific International

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

Create a Framework for the Medical Devices Regulation (MDR)

Josephine Tolley
Regulatory Affairs
Johnson & Johnson

9:30

Review the Do’s and Don’ts of Transitioning into the New Medical Devices Regulation (MDR)

Robert Steele
Executive Vice President Quality Assurance, Regulatory and Clinical Affairs
Convatec

10:15

Networking and Refreshment Break

10:45

Evaluate the New Responsibilities of Stakeholders in the Supply Chain

Hilde Viroux
Director EURMEA RA, MD & Vision Care
Alcon

11:30

Implement MDR Guidelines While Submitting to Notified Bodies

Paul Sim
KS Medical Devices Knowledge Manager
BSI Group

12:15

Networking Luncheon

13:30

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

14:15

Examine the Impact of GDPR on the Medical Device Industry

Elisabethann Wright
Partner
Hogan Lovells

15:00

Networking and Refreshment Break

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

15:30

The First Major Change of MTE Code —
Best Practices for Supporting Third Party Medical Education according to the new MedTech Europe Code of Ethical Business Practices

Dr. Heidi K. Jauch
Vice President Compliance Officer EMEA
Zimmer Biomet EMEA

16:15

The Second Major Change of MTE Code —
The Transparency Disclosure Requirement

Suzanne Durdevic
Senior Director, General Counsel Europe EMEA
Boston Scientific International

17:00

Close of Conference

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