Job Description

• Perform all MOH required tasks related to Registration of pharmaceuticals, Medical Devices and food supplements. • Ability to insert new molecules and dosage forms in IDL • Ensures that current registration requirements are available, communicated and implemented • Compiles and submits registration files for new products • Follow-ups with the Iranian Ministry of Health on files review and ensure timely submission of additional documentation requested • Compiles and submits renewal files and updates of approved products • Proof-reads labeling items • Responsible for GMPs and external inspection by competent authorities • Responsible for authorization for distribution for imported shipment based on local regulations