Live Chat Software
January 22 - 24, 2018
United States

MAIN CONFERENCE DAY TWO

8:00 am - 9:00 am REGISTRATION AND MORNING JUMPSTART

Julian  Goldman, Director of the Program on Medical Device Interoperability at Massachusetts General Hospital, Harvard Medical School

Julian Goldman

Director of the Program on Medical Device Interoperability
Massachusetts General Hospital, Harvard Medical School



Anthony Watson, (Former Director, Division of Anesthesiology, General Hospital Infection Control, and Dental Devices, FDA) Associate Vice President, Regulatory Affairs - Devices at Sanofi

Anthony Watson

(Former Director, Division of Anesthesiology, General Hospital Infection Control, and Dental Devices, FDA) Associate Vice President, Regulatory Affairs - Devices
Sanofi

•Join leading regulatory experts at this panel to evaluate Issues related to strategic implications of FDA device regulations
•Hear best practices for compliance with ISO 13485:2016
•Prepare yourself for the new EU Medical Device Regulations (EU MDR)
•Evaluate how MDUFA IV would impact the path to FDA approvals 
Pat Baird, Head of Global Software Standards at Philips

Pat Baird

Head of Global Software Standards
Philips

Robert Ezzell, Associate Director , Global Regulatory Affairs - Medical Devices at Sanofi

Robert Ezzell

Associate Director , Global Regulatory Affairs - Medical Devices
Sanofi

10:45 am - 11:00 am MORNING MINGLE

•Experience that both quality and safety are improved when the software  development team is agile, and that regulatory requirements can still be met

•Delve into several key areas for applying Agile methods in the medical device context

•Fit together hardware and software development, and being Agile in both
Nancy Van Schooenderwoert, President and Managing Partner at Lean-Agile Partners

Nancy Van Schooenderwoert

President and Managing Partner
Lean-Agile Partners

Brian  Shoemaker, Principal Consultant at ShoeBar Associates

Brian Shoemaker

Principal Consultant
ShoeBar Associates

12:00 pm - 1:00 pm NETWORKING LUNCHEON

1:00 pm - 1:45 pm MEDICAL DEVICE SOFTWARE - REQUIREMENTS AND CONFIGURATION MANAGEMENT


1:45 pm - 2:30 pm EXPLORE WHAT’S NEXT IN HUMAN FACTORS ENGINEERING FOR MEDICAL DEVICE MOBILE APPS AND IOT

•Evaluate Chances and Risks of Mobile Health Apps
•Delve into best practices in Human Factors for Medical Device Mobile Apps
•Uncover IoT Opportunities and hear examples of potential features  for Medical Device Mobile apps
Ed Israelski, Advisor on Human Factors, Combination Product Development, Former Director Human Factors at AbbVie

Ed Israelski

Advisor on Human Factors, Combination Product Development, Former Director Human Factors
AbbVie

2:15 pm - 2:45 pm Afternoon Recharge - Network over Refreshments

2:15 pm - 3:00 pm Actionable Data Collection and Analytics to Reduce Operating Costs



· Understand the value of passively collected data
·Implement a predictive analytics approach
·Reduce operating costs, increasing inventory turns, and identifying risks turns, and identifying risks


Patrick Schenkel, Business Intelligence Manager at Zimmer Biomet

Patrick Schenkel

Business Intelligence Manager
Zimmer Biomet

3:15 pm - 4:00 pm INCORPORATE IOT AND INTEROPERABILITY TO ENABLE DATA FOR YOUR MEDICAL DEVICE SOFTWARE


David Arney, Lead Engineer, MD PnP Program at Massachusetts General Hospital

David Arney

Lead Engineer, MD PnP Program
Massachusetts General Hospital

4:00 pm - 4:05 pm CHAIRS’ CLOSING REMARKS