Products’ registration at MOH. Responsible for preparing and compiling registration documentation. Liaising and negotiating with regulatory authorities. Follow up till completion of registration process. Ensuring compliance with regulations set by MOH. Keeping up to date with changes in regulatory legislation and guidelines of MOH. Knowledge of FDA and CE regulations. Knowledge of European standards regarding equipments and medical devices (and similar) Advise sales teams on eligible exported products. Import permit. Release of imported goods. Follow up on samples for analysis.
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