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About
Streamlined Medical Device Registration Process
Registering your medical device in Bangladesh requires navigating complex regulations and guidelines. Zivadra’s experienced team simplifies the process, offering full support to ensure that your device meets the requirements of the DGDA. Our services include document verification, application submission, and regulatory consulting, providing you with a seamless path to market approval. Let us handle the registration process, so you can concentrate on growing your business. Contact us today to learn more!Interact
