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Market Access and Reimbursementof Innovative Medical Devices and IVD in Europe
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...Continue reading
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Issues to be covered
- 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.
Who should attend
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.
About The Lecturer
