A practical overview of the documents and regulatory considerations when a foreign manufacturer changes its Bangladesh local agent.
Yes, but the change should be handled through the appropriate regulatory process because the local representative or registration holder is connected to the product registration.
A planned transfer helps reduce disruption to registrations and future regulatory activities. A duplicate-certificate issue fee or additional requirements may apply depending on the case.
MedTech supports manufacturers with regulatory documentation, registration and Bangladesh market access. Requirements may change, so confirm the current DGDA requirements for your specific product before submission.
Kiara Foster
Head of Content
Kiara
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