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Medical Devices Registration in Bangladesh - Chengdu


Post #: A45204595
Posted By: mavenprofserv (mavenprofserv ads)
Posted on: 11 April
Reply to: (Use contact form below)
Ad Type: Offering
 

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. Operating under the Ministry of Health and Family Welfare, DGDA regulates the import, production, distribution, and sale of medical devices, emphasizing quality and safety standards. 

https://mavenprofserv.com/medical-devices-registration-in-bangladesh/

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MDR
MedicalDeviceTechnicalFile
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Medical Devices Registration in Bangladesh - Chengdu Professional Services




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