Job Description
- Handling process of registration of food supplements and herbal medicines, and preparing PMF/CTDs SOPs, specifications, certificates Consumer Information, literature searches, and other regulatory activities.
- Be familiar with international pharmaceutical guidelines and pharmacopeia.
- To monitor and control all necessary manufacturing, packaging, associated documents, test and release of the produced batch of the pharmaceutical product, and compliance with the requirements of Good Manufacturing Practice.
- Acting as a link between companies and Iran MOH, ensuring that products are manufactured and distributed in compliance with appropriate legislation
- The approval and monitoring of contract manufacturers and providers of the other GMP related outsourced activities.
- To implement and manage MOH regulations in the company