Starting from the 1 of January 2020 registration of medical devices in Russia will be available according only to Eurasian Economic Union (EAEU) requirements. It means that now for registration classes IIB, III medical devices and implantable devices producer must conduct a multicenter clinical trial. More than 10.000 medical devices in Russia will face such requirements in the nearest future.
X7 Research offers its clients full accompaniment and support at all stages of conducting multicenter clinical trials in Russia, EAEU, CIS and EU.
BUDGETING OF CLINICAL STUDIES FOR MEDICAL DEVICES
SUPPORT AT ALL STAGES OF STUDY
X7 Research team has decades of experience in conducting multicenter studies. We will be glad to consult you about registration or clinical trial budgeting for your medical device.
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