In Partnership with:
Examine Game Changing Technologies, Industry Guiding Regulations, and Ground Breaking Innovations
“Always fun and informative”
– Human Factors and Accessible Medical Technology Specialist, FDA
Today a software revolution is happening in the medical device industry. As hardware becomes more powerful and more affordable, expanded capabilities and differentiation are being designed into the software. Devices are now linked to smartphones and tablets to provide real-time data, enhancing the clinical and patient experience. In order to survive in this highly regulated and competitive market, companies must move one step ahead of emerging trends by selecting new and innovative software design technologies that are in line with the latest regulations and track where the industry is going.
We designed compelling content streamed through interactive panel/roundtable discussions, case studies, keynote sessions, a one of a kind off-site visit to MD PnP Labs of Massachusetts General Hospital, Harvard Medical School - and other interactive program formats led by the industries brightest minds. All designed for you take back valuable insights and instruction to your organization, manufacturing facility, hospital, and research lab.
Testimonials
Top Benefits of Attending:
Address the latest regulatory requirements related to UDI, human factors cybersecurity, MDUFA, MDR and IVDR
Learn how to reduce medical device costs by using an effective software development strategy while improving speed to market
Establish quality assurance processes, techniques & controls throughout the development lifecycle
Improve Cyber Security & Risk Management Strategies to bolster patient privacy and protection
Increase Interoperability & Connectivity between systems and across devices to maximize the use of big data and analytics
Explore how to better utilize Human Factors engineering and collaborate with different stakeholders including physicians, patients and drug manufacturers to improve user experience
Featured Speakers
Director of the Program on Medical Device Interoperability
Massachusetts General Hospital, Harvard Medical School
(Former Chief of General Hospital, Devices Branch, FDA) Senior Director, Sanofi Medical Device Software Factory
Sanofi
Head of Product, Healthcare & Life Sciences, Google Cloud
Deputy Chief Information Security Officer
Partners Healthcare
Head of Global Software Standards
Philips
Director of Innovation
Blue Cross Blue Shield of Massachusetts
(Former Director, Division of Anesthesiology, General Hospital Infection Control, and Dental Devices, FDA) Associate Vice President, Regulatory Affairs - Devices
Sanofi
Connected Sensing Venture Business Leader
Philips
Director of Bioengineering
Brigham and Women's Hospital
Business Intelligence Manager
Zimmer Biomet
Advisor on Human Factors, Combination Product Development, Former Director Human Factors
AbbVie
Global Product Security & Services Officer
Royal Philips
Principal Consultant
ShoeBar Associates
Lead Engineer, MD PnP Program
Massachusetts General Hospital
President and Managing Partner
Lean-Agile Partners
Global Head of Product Development, CTO
Cerner Health Services (Formerly Siemens Health Services)
Associate Director, Software Quality Assurance
Foundation Medicine Inc.
Associate Director , Global Regulatory Affairs - Medical Devices
Sanofi
Biomedical Cybersecurity Specialist, eCare Biomedical Device Integration Team
Partners Healthcare
Director, Healthcare
RTI
Consultant
CIMIT
