San Francisco Bay Area In Person Event: IVD Regulatory Overview and Updates


This seminar is planned to provide a general overview of the EU IVDR conformity assessment, a summary update of IVD related regulatory updates. Due to the diverse background of the audience, time will be allocated for answering attendee questions.
Registration Fees & Deadlines
Free
Agenda
General regulatory update, focusing on IVD devices (e.g. IVDR transitions, CDx, LDT) High level overview of IVDR conformity assessment Q&A
Speakers
Balazs Bozsik
Technical Director - Medical Audit, SGS North America
Daniel Fisher
Regional Sales Manager - Medical Devices at SGS
Location
Fogarty Innovation
2495 Hospital Drive
Suite 300
Mountain View, California 94040
Sponsors
Fogarty Innovation
Event Location Sponsor
SGS
Event Sponsor
Platinum Chapter Sponsors
MDSS
RxTROSPECT
Cancellations and Refunds
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation. All cancellation requests must be submitted in writing to support@raps.org. Cancellations will receive a full refund minus a 20% administrative fee. RAPS is unable to accept cancellations by phone.
Substitutions
Paid registration substitutions may be accepted with written approval from RAPS for requests received before the start of the event. To transfer a registration, email support@raps.org with the event title, name of the original registrant and the contact information for the new attendee.
Proof of Attendance
A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.