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TZID:America/New_York
X-LIC-LOCATION:America/New_York
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TZOFFSETFROM:-0500
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DTSTART:19700308T020000
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BEGIN:VEVENT
UID:2140535:Event:66646
DTSTAMP:20260523T060701Z
SUMMARY:Webinar On Preventing Medical Device Recalls
DESCRIPTION:Description : The secret to preventing medical device reca
 lls is to implement and follow basic practices for specifications and 
 design control, design for process reliability, production validation 
 and design validation using accelerated life tests. This webinar is ab
 out controlling safety risk from specification writing to device retir
 ement – control throughout the product’s life cycle. In a recent s
 tudy, the FDA has reported a 95% increase in medical device recalls ov
 er a nine year period ending in 2014 attributable to a variety of reas
 ons. Whatever the reason, medical device recalls are expensive and mos
 t importantly carry significant risk to the health and safety of patie
 nts. The increase indicates serious failures in the processes and cont
 rols designed to ensure reliability, safety, and effectiveness of the 
 recalled devices. As medical devices become more complex and software 
 components become more critical to device functioning, the need for pr
 oactive risk prevention becomes more and more evident. The webinar wil
 l provide an overview and a foundation for further learning concerning
  preventing recalls during specification writing, risk assessment and 
 risk management, preventing recalls during the early design and the de
 tail design phases of development, and preventing recalls during valid
 ation, verification, and software design. Areas Covered in the Session
  : Preventing recalls during specification writing Preventing recalls 
 during early design Preventing recalls during the detail design phase 
 Designing for Prognostics to protect patients Preventing recalls durin
 g production validation Preventing software design recalls Preventing 
 supply chain quality defects to avoid recalls Preventing recalls using
  a verification process Preventing recalls using the design validation
  process Role of management in preventing recalls Innovative methods u
 seful in preventing recalls Who Will Benefit: Quality Professionals Re
 gulatory Professionals Manufacturing & Design Engineers Compliance Dep
 artments Research & Development Teams Documentation Personnel Complain
 t Handling Personnel Product Development Teams\n\nFor more information
  visit https://medtechiq.ning.com/events/webinar-on-preventing-medical
 -device-recalls
DTSTART;TZID=America/New_York:20150824T130000
DTEND;TZID=America/New_York:20150824T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=MD1467
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=MD1467
CONTACT:4169154458
ORGANIZER:Compliance Trainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
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