A Three-Day Training Program on Good Manufacturing Practices (GMP) and Pharmaceutical Risk Management Commences
The Food and Drug Authority of the Ministry of Public Health, in collaboration with the World Health Organization (WHO), has launched a three-day training program titled "Good Manufacturing Practices (GMP) and Pharmaceutical Risk Management" in the Authority main conference hall.
The training program is being conducted to enhance the technical capacity of 35 staff members and specialists from the Directorate of Pharmaceutical and Health Products Evaluation and Registration, strengthen quality assurance systems, improve pharmaceutical manufacturing processes, and promote the implementation of international standards within the country's pharmaceutical industry.
The program covers the importance of implementing GMP standards, quality management systems, principles of documentation and record-keeping, pharmaceutical manufacturing equipment and facility requirements, standard warehouse management, storage of raw materials, dispensing and preparation of starting materials, manufacturing principles for various pharmaceutical dosage forms, sterilization techniques, quality control, pharmaceutical risk management, and other technical GMP requirements.A Three-Day Training Program on Good Manufacturing Practices (GMP) and Pharmaceutical Risk Management Commences
The Food and Drug Deputy Ministry of the Ministry of Public Health, in collaboration with the World Health Organization (WHO), has launched a three-day training program titled "Good Manufacturing Practices (GMP) and Pharmaceutical Risk Management" in the deputy ministry's main conference hall.
The training program is being conducted to enhance the technical capacity of 35 staff members and specialists from the Directorate of Pharmaceutical and Health Products Evaluation and Registration, strengthen quality assurance systems, improve pharmaceutical manufacturing processes, and promote the implementation of international standards within the country's pharmaceutical industry
The program covers the importance of implementing GMP standards, quality management systems, principles of documentation and record-keeping, pharmaceutical manufacturing equipment and facility requirements, standard warehouse management, storage of raw materials, dispensing and preparation of starting materials, manufacturing principles for various pharmaceutical dosage forms, sterilization techniques, quality control, pharmaceutical risk management, and other technical GMP requirements. These topics will be delivered through both theoretical and practical sessions.
