Job Description
• Follow-ups with the Iranian Ministry of Health on files review and ensures timely submission of additional documentation requested
• Supervision of quality processes
• Familiar and provision of SOPs
• Gathering Pharmacovigilance and ADR reports
• Develop professional relationships with MOH staff and proactively monitor relevant governmental bodies to identify changes in legislation/regulations
• Review documents as CTD, PMFs, to fulfill MOH requirement for registration
• Familiar with TTAC portal of MOH and material registration.
• Review product printing materials, labeling, specification sheets with applicable regulations and policies.