![Good Manufacturing Practices [cGMP]](/web/image/slide.channel/78/image_1920/Good%20Manufacturing%20Practices%20%5BcGMP%5D?unique=b4d5675)
Good Manufacturing Practices [cGMP]
In- Person / Virtual
Who Should Attend?
THIS BROADLY BASED COURSE IS INTENDED FOR ALL SCIENTISTS AND TECHNOLOGISTS CONCERNED WITH THE DEVELOPMENT PROCESSING OF PHARMACEUTICAL PRODUCTS, AND WITH RELATED DRUG REGULATORY AFFAIRS
THIS BROADLY BASED COURSE IS INTENDED FOR ALL SCIENTISTS AND TECHNOLOGISTS CONCERNED WITH THE DEVELOPMENT PROCESSING OF PHARMACEUTICAL PRODUCTS, AND WITH RELATED DRUG REGULATORY AFFAIRS
Course Topics:
• Quality Systems
• Laboratory System
• Infrastructure: Facilities, Utilities, Equipment
• Materials and Supply chain management
• Non-Sterile Manufacturing Systems
• Sterile Manufacturing Systems
• Filling, Packaging, Labeling
• Product Development
• Product Development
Number of Sessions :
10 Sessions
Instructor:
SPEAKER
Dr. Mohamed Ibrahim
Deputy Quality Manager- Kimal
SPEAKER
Dr. Nabil Mofeed
Senior Supervisor of R&D stability labs at Al-Andalous Pharmaceut
Speaker
Dr. Mohamed Saad
Pharma consultant, VALOR GM
.