December 2024

In the pharmaceutical, cosmetics, and medical device, regulatory dossier plays a very significant role in securing registration and product approval […]

 Electronic common technical documents (eCTD) has become global standard for regulatory submissions. eCTD submission has revolutionized the process of drug

Common technical document (CTD) is a harmonized format of documents that is recognized globally across the world for submission of

If you are looking for authorized agent or representative for your medical device registration, you are on right platform. Medwisdom