OVERVIEW DOWNLOAD:
5th Annual Medical Device Global Post-market Surveillance Conference

January 30-31, 2019 | Alexandria, VA

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ABOUT THE CONFERENCE

The medical device industry is consistently challenged to provide uninterrupted product quality throughout the product lifecycle in order to ensure the patient’s safety. Postmarket surveillance executives utilize large quantities of performance data collected for a plethora of sources including patients, healthcare providers, product literature reviews and social media to continuously monitor a medical product’s functionality. This compiled data allows executives to analyze product performance to reveal potential malfunctions and inconsistencies ensuring manufacturers are able to institute the needed corrective actions, which can mitigate the potential for serious medical repercussions for patients.

Continuing to build on the success of our Annual Medical Device Postmarket Surveillance Conferences, this program’s fifth annual iteration will continue to provide an unrivaled opportunity for networking, education and knowledge share in an environment which is continually evolving, and in a market place which is highly competitive and strictly regulated. Designed for medical device and diagnostic companies alike, this two-day executive level meeting will provide participants with extensive, in-depth learning and knowledge share highlighting a range of topics including EU MDR postmarket compliance updates, complaint escalation processes and the exploration of regulatory requirements on a global scale.

TOPICS TO BE ADDRESSED INCLUDE:

  • Compliance Update: Reviewing EU MDR requirement deadlines
  • Streamlining MDR filing processes to ensure regulatory compliance
  • Notified Body Perspective: Navigating EU MDR impact on PM operations
  • Impact of increased scrutiny regarding medical device software patching
  • Panel: Importance of cybersecurity initiatives in securing product quality
  • Intricacies of compliant benefit-risk ratio development strategies
  • Advancing internal use of postmarket data and analyses
  • Continuous monitoring solutions to ensure uninterrupted safety monitoring
  • Strengthening product postmarket escalation process for malfunctions
  • Integrating literature reviews in postmarket product data compilation
  • Navigating the use of social media as a compliant postmarket data source
  • Building postmarket filing compliance through the development of templates
  • Maintaining compliance while employing lean complaint handling strategies
  • Utilization of medical device registries in postmarket operations
  • Data overload: Determining the appropriate level of data needed for PM analyses
  • Postmarket strategies to ensure employment of seamless recall management procedures
  • Exploration of postmarket data requirements on the global and regional scale

ABOUT THE CONFERENCE

Continuing to build on the success of our Annual Medical Device Postmarket Surveillance Conferences, this program’s fifth annual iteration will continue to provide an unrivaled opportunity for networking, education and knowledge share in an environment which is continually evolving, and in a market place which is highly competitive and strictly regulated. Designed for medical device and diagnostic companies alike, this two-day executive level meeting will provide participants with extensive, in-depth learning and knowledge share highlighting a range of topics including EU MDR postmarket compliance updates, complaint escalation processes and the exploration of regulatory requirements on a global scale.

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