Brief Introduction about yourself
Preparation and review of Dossiers and related Documents for Product Registrations as per the CTD, ACTD, eCTD, and National Guidelines. Responsible for the complete process from Receiving of the Product until the Registration in the Specific Country Handing of FDA Queries, Reviewing and Updating Documents received from the Plant, Arranging the Registrations Samples/Admin Docs, Liaoning with the Buyers Regulatory Department for timely and smooth registration.
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