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4th Annual Medical Device Safety Monitoring & Reporting

Establishing a Cross-Market Reporting Model to Optimize Medical Device Management

27-28 Jan 2016
Platinum Hotel - Las Vegas, NV, United States of America


Why You Should Attend

4th Annual Medical Device Safety Monitoring & Reporting

Recent focus has been placed on the medical device industry in reviewing its capacity to evaluate, monitor and alert users of safety concerns related to the specific devices. Although significant efforts are underway to change this and facilitate sounder medical device reporting and electronic medical device reporting, companies are still struggling with identifying what the international and national regulatory bodies are requiring.

This timely conference will bring together Regulatory & Quality professionals to address key updates and advancements in medical device safety, medical device reporting, eMDR, post market-surveillance, complaint handling, audit handling, and national & international standards.

Key Topics

  • Develop a Cohesive Global Reporting Model that Will Comply with FDA and ISO Standards
  • Implement a Robust Electronic Medical Device Reporting (eMDR) Program to Acheive FDA MDR Compliance
  • Remain Vigilant with Post Market Surveillance Data Accumulated to Ensure All Generated Information is Documented
  • Manage Complaint Handling Effectively to Ensure Accurate Data Accumulation
  • Reduce Risk in the Front End to Ensure Compliant Reporting
  • Previous Attendees Include

    Omnyx, LLC, Stryker Medical, St. Jude Medical, Fresenius Medical Care North America-Global Manufacturing Operations, Novocure, Covidien Surgical Solutions, Cardinal Health, Allergan, Abbott Medical Optics, Inc., Boston Scientific CRM, Terumo BCT, Food & Drug Administration/Office of Regulatory Affairs and many others


    Why Choose marcus evans?

    marcus evans specialises in the research and development of strategic events for senior business executives. From our international network of 63 offices, marcus evans produces over 1000 event days a year on strategic issues in corporate finance, telecommunications, technology, health, transportation, capital markets, human resources and business improvement.

    Above all, marcus evans provides clients with business information and knowledge which enables them to sustain a valuable competitive advantage and makes a positive contribution to their success.




    Event Partners


    Practical Insights From

    Bill Maloney
    Physicist, MDR Policy Branch - Office of Surveillance and Biometrics Center for Devices and Radiological Health
    Food and Drug Administration

    Jose Lima
    Vice President, Quality
    Endologix

    Darin S. Oppenheimer, RAC
    Director, Global Regulatory Affairs
    Baxter Healthcare Corporation

    Dick Roy
    Product Surveillance Director
    GE Healthcare

    Karen Smith
    Director of Regulatory Compliance
    BD MPS

    Khaudeja Bano, M.D.
    Senior Medical Director, Medical Device Safety Head
    AbbVie Inc.

    Malik Khan
    Quality Manager
    Stryker - Endoscopy

    Click Here For Full Agenda

    Voice of Our Customers
    • "The greatest benefit of marcus evans conferences is strong representation from industry and the time set aside for question and answer, panel discussions, and networking." - Abbott Molecular
    • "Smaller conferences encourage more in-depth discussion which is liked. Quality of speakers top-notch." - Olympus Biotech Corporation
    • "The conference was very well done. Very well organized. I have attended numerous and I would put this in my top 5." – Health Troncis
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    Event Contact

    For all enquiries regarding speaking, sponsoring and attending this conference contact:

    Tyler Kelch


    455 N. Cityfront Plaza Dr.
    9th Floor
    Chicago, IL 60611

    Telephone:
    312-894-6310
    Fax: 312-894-6304
    Email: Tylerke@marcusevansch.com