Reviewing & compiling dossiers for registration/re-registration of products
Following up actively on all dossier submissions
Endeavoring constantly to anticipate and respond to regulatory/ technical queries
Achieving timely market driven product submissions and registration approvals.
Ensuring compliance with Ministry of health regulations in U.A.E, G.C.C.
Keeping up to date with changes in regulatory legislation and guidelines
Preparing submission of variations and renewals
Outlining the requirements for labeling, storage and packaging
Preparation of registration dossiers in CTD Format.
Maintaining the internal document system for compliance to regulatory submissions.
Meeting product re...
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