Session Sponsors Industry Partner
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Contact Us
[email protected] 917.338.6822 917.210.1075 |
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Greetings!
Any lag in getting products to market is costly on every front from cash expenditures to loss of market share and the evaporation of the first-to-market competitive edge. Designing medical devices that meet the complex safety certification and regulatory requirements are the most common reasons for delays, especially if these requirements are not known in the early stages of design. With the transition to the 3rd Edition of IEC 60601 globally, the approval process is expected to be more challenging and time consuming than ever. Are you ready for the transition? Do you understand the new requirements? The Medical Devices Conference taking place on November 5-7 in San Francisco will put you in front of regulatory and Notified Bodies' officials and experts who will provide you with such guidance to speed your time to market and smooth the transition to IEC 60601.
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Meet key decision-makers and hear from a distinguished speaker faculty that includes:
- Richard Chapman, General Engineer, Center for Device and Radiological Health (CDRH), FOOD AND DRUG ADMINISTRATION (FDA) (pending)
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Steve McRoberts, Principal Engineer for Medical Regulatory & Proprietary Compliance, UNDERWRITER LABORATORIES
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Justin Heyl, Program Manager, INTERTEK CONSULTING SERVICES
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Dale Hallerberg, Technical Manager - Medical Test, T�V RHEINLAND NORTH AMERICA
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- Abe Mamaghani, Manager Development R&D, ABBOTT LABORATORIES
- Arnab Ray, Research Scientist, FRAUNHOFER CENTER FOR EXPERIMENTAL SOFTWARE ENGINEERING
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- Sathish Ramkumar, Sr. Development Manager, Software Development, Imaging Clinical Applications and Platforms (ICAP)-NM, PHILIPS HEALTHCARE
- Ron Rammage, PMP, Software Engineering Manager, ABBOTT MEDICAL OPTICS
- Juergen Stettin M.D., Ph.D. , CEO, PROSYSTEM AG, Hamburg; Chairman of German Scientific Hospital Organization (WGKT)
- Oliver P. Christ, CEO Healthcare PROSYSTEM AG, Hamburg; Member of International Standardization Group for IEC 62366
- Thomas L. Bento, Sr. Regulatory Consultant, CERTIFIED COMPLIANCE SOLUTIONS, INC.
- Brian Shoemaker, Principal Consultant, SHOEBAR ASSOCIATES
- Tajudeen Oladele, Consultant-Global Regulatory Compliance, TERUMO CADIOVASCULAR
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To register, call Sam Eid at 917 338 6822 or email [email protected]. For any other inquiries, please contact Judy Tsui at 917 210 1075 or at [email protected].
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