With medical device safety playing a critical role in healthcare, it is significant for organizations to ensure effectiveness by implementing a safety action plan to ensure success for the product. Medical devices are paramount when providing care to patients; however, they occasionally fail to operate OR are misused causing further harm to the patient or even death, which makes risk assessment and device reporting important junctures during development. All parties that are involved during the life cycle of the medical device outside the organization including government, manufacturer, vendor, and user facilities must be transparent and communicate properly to reduce risk and further advance into the marketplace.
Speakers: Michael Drues, Edward Reverdy, Deva Puranam, Anupama Govindarajan, Khaudeja Bano, Lawrence Perruzza, Michael Hunn, Lillian Kirk
Time: 8:00 am - 3:45 pm
Early Bird Pricing-Register by February 8, 2019: USD 1895.0,
Standard Pricing: USD 2095.0,
Onsite Pricing: USD 2195.0
Medical Device Safety and Reporting Summit
Reviews are public and modifiable.
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