We help you to prepare Medical Device Technical File (MDR) as per the regulatory requirement of EU MDR 745/2017 and submit to notified body for review and approval of CE certification. In Bangladesh, the Directorate General of Drug Administration (DGDA) oversees medical devices registration. .
https://mavenprofserv.com/medi....cal-devices-registra
MedicalDevicesRegistrationinBangladesh
MedicalDevicesRegistration
MDR
MedicalDeviceTechnicalFile
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