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مهارتهای ارتقاء دانش فنی داروسازی
- methods of good manufacture practice GMP
- quality management system
- methods of good storage practice GSP
- methods of good distribiution practice GDP
- Management of quality risks in the pharmaceutical industry
- Corrective and preventive action with risk management approach (CAPA).
- Validation of analysis methods according to guidelines ICH Q10
- Validation of processes in pharmaceutical industry
- Writing a comprehensive file for chemical drugs acording to CTD pattern
- Writing a comprehensive file for manufacturing food and dietary supplements PMF
- Writing a comperhensive file for manufacturing herbal and traditional medicine DMF
- Validation of systemic documents in pharmaceutical industry21CFR
- introducing the formulation of different pharmaceutical dosage forms
- Introduction various type of devices and lines related to producing and packaging different pharmaceutical dosage form
- Introducing various type and usage of excipients and ingredient which common in producing different dosage forms
- Introducing various Methods for producing different pharmaceutical dosage forms
- Introducing equipment and supplies of pharmaceutical laboratory