Unique Skill ID: KS1225377HQ9VXS4TT2D

Common Technical Document

Common Technical Document (CTD) is a regulatory requirement for submission of drug and biologic product applications to regulatory authorities in many countries. It is a specialized skill as it involves the preparation and organization of large volumes of technical information, including clinical and non-clinical data, product quality data, and regulatory documentation. A CTD submission requires expertise in scientific writing, regulatory requirements, and project management to ensure that the submission meets the requirements of the regulatory agency and is completed within the specified timelines.

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