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Designing Medical Devices for Patient Safety - Webinar By ComplianceOnline
1 Seiten
Veröffentlicht von
Tim Linen
Why Should You Attend: Medical devices represent a significant sector of the U.
S.
healthcare industry, with annual sales exceeding $13 billion.
These devices,
including pacemakers, cardiac defibrillators, infusion pumps, and neural...
[Mehr]
Why Should You Attend: Medical devices represent a significant sector of the U.
S.
healthcare industry, with annual sales exceeding $13 billion.
These devices,
including pacemakers, cardiac defibrillators, infusion pumps, and neural
stimulators, have unacceptably high failure rates.
Missing safety requirements in
the product specification are often the source of harm to patients.
For next-generation devices, which are much more complex, we must include
robustness requirements in the specifications through hazard analyses during the
concept stage.
FDA approval hinges on demonstrated safety and the reliability of
the safeguards.
Including safety requirements early reduces the time to market.
Attend this webinar to learn how you can design medical devices that ensure patient
safety.
We will also review hazard analysis techniques and safety design techniques
for devices, including next-generation ones.
Areas Covered in the Seminar:
Dangers to patients from medical devices.
Inhere
[Weniger]
Schlagworte
complianceonline,
dangers,
design,
devices,
event,
events,
http,
including,
itevent,
medical,
patient,
patients,
requirements,
safety,
technology,
training,
webinar
