חדש

Market Access and Reimbursementof Innovative Medical Devices and IVD in Europe

מרצה: Dr. Tilo Mandry, Mr. Michael Weisser
גרסה להדפסה

שתף קולגה:

מקוון - בזום

Ensure the commercial success of your product!

Set the right course during development

Managers & senior staff from companies that intend to bring innovative medical devices or in vitro diagnostics (IVD) to the European markets are invited to join this essential webinar.

The developers of such products...המשך קריאה

Ensure the commercial success of your product!

Set the right course during development

Managers & senior staff from companies that intend to bring innovative medical devices or in vitro diagnostics (IVD) to the European markets are invited to join this essential webinar.

The developers of such products face two major challenges: Strict safety and efficacy requirements must be met to bring the innovation to market at all.

At the same time, it has become difficult to get an innovative medical device or IVD reimbursed by the European public healthcare systems, as they place high demands on demonstrating clinical benefit.

This webinar shows how to meet the requirements for both market access and successful commercialization through timely planning. The focus is on the right study design, which is crucial for obtaining the CE mark and for commercial success.

Case studies will be used to show how innovative medical devices and IVD can be successfully brought to European patients, what role the CE mark plays in commercialization, and how the major European countries differ in terms of benefit assessment.

הרשמו כבר עכשיו ללא עלות
ההשתתפות מותנית בהרשמה מראש

סגור
תאריך:  יפורסם בקרוב.
הקורס יפתח על פי רמת ההתעניינות בנושא.

מתעניינים? לחצו כאן

    מיקום הקורס: הוובינר מועבר באמצעות Zoom
    משך הפעילות: כשעה
    שעות: 16:00 - 15:00
    נקודות זכות: 0
    שפת הקורס: English

    יש לך שאלה? יש לנו את כל התשובות

    מה תכני הקורס?

    • Overview of the European Med Tech market (market size, key countries, health economic key data (spending on health care, etc.)
    • CE-Mark to receive market access and the meaning of reimbursement
    • Pathways for reimbursement in the European key countries (Germany, France, UK, Spain, Italy):
    • Health Technology Assessment Procedures
    • Reimbursement In the in-patient sector: purchasing power of hospitals, reimbursement via DRG, reimbursement medical devices via pathways for highly innovative products
    • Reimbursement in the out-patient sector: procedure to get listed in the directory for reimbursed medical devices and auxiliary goods. Pathways for innovative medical devices etc.

    למי זה מתאים?

    Medium-sized medical device companies with an existing medical device portfolio or with medical device prototypes in the late development phase (about one to two years before product launch). Companies with little or no experience of reimbursement in Europe.

    מי מעביר את הקורס?

    Tilo Mandry
    Tilo Mandry, Lead International Liaison Manager, IGES, supports international medical
    קרא עוד
    Michael Weisser
    Michael Weisser, CEO of AiM (an IGES Group company), has
    קרא עוד

    הוספת תגובה

      אנא חזרו אלי