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Inside Medical Technology

11 - 12 April 2018 // Nuremberg, Germany

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Exhibitors & Products MT-CONNECT 2018

What requirements do clinical trials have to meet? How does a product become reimbursable? How does the conformity assessment procedure work? Representatives from the Federal Institute for Drugs and Medical Devices (BfArM) and the Federal Joint Committee (G-BA), with regard to Medicinal Products and Medical Devices (ZLG) will be available for one-on-one discussions about the path of an innovation from research to supply.

One-on-one discussions can be booked via or directy at hall 10.0/booth 309.

Presentation of the National Medical Technology Information Platform

LOGO_Presentation of the National Medical Technology Information Platform

One-on-one discussions is assigned to following product groups:

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