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Congress Center Basel

2018年4月17日 (火) 午後 2:00 - 2018年4月19日 (木) 午後 11:00

Messeplatz 21 , CH-4021 Basel , SWITZERLAND

DIA EUROPE 2018

Challenges in the Current Regulatory Landscape Considering FDA and MDR Expectations

Session Chair(s)

Shayesteh  Fürst-Ladani, MBA, MS

Shayesteh Fürst-Ladani, MBA, MS

CEO

SFL Regulatory Affairs & Scientific Communication, Switzerland

Challenges in the Current Regulatory Landscape Considering FDA and MDR Expectations

Speaker(s)

Niall  MacAleenan

A European Regulatory Authority Perspective on the New EU Device Regulations

Niall MacAleenan

Health Products Regulatory Authority (HPRA), Ireland

Medical Device Lead/Clinical Assessment and Policy Manager

Karin  Schulze, DrSc

How MDR Impacts Medical Device Manufacturer?

Karin Schulze, DrSc

SFL Regulatory Affairs & Scientific Communication, Switzerland

Head Medical Devices

Murray  Malin, MD, MBA

Industry Preparation to Comply with the FDA and MDR/IVDR Regulatory Requirements

Murray Malin, MD, MBA

Abbvie, United States

Medical Director

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