Guidelines for the Submission of Bangladesh Common Technical Document

These guidelines provide instructions for applicants preparing a Common Technical Document (CTD) for the registration of medicines for submission to the Directorate General of Drug Administration (DGDA). The document describes how to organize applications based on the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) guidelines on the CTD. The CTD is currently applicable only to human, not veterinary, medicines.

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