In the pharmaceutical, cosmetics, and medical device, regulatory dossier plays a very significant role in securing registration and product approval from domestic and international regulatory authorities. Regulatory dossier provides a well structured representation of product data and compilation of

Electronic common technical documents (eCTD) has become global standard for regulatory submissions. eCTD submission has revolutionized the process of drug approval and registration. This standardized format of eCTD has simplified the communication between pharmaceutical companies and regulatory bodi