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Good Manufacturing Practices [cGMP]

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Cairo, Egypt

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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

Course Topics:

• Quality Systems
• Laboratory System
• Infrastructure: Facilities, Utilities, Equipment
• Materials management
• Non-Sterile Manufacturing Systems
• Sterile Manufacturing Systems
• Filling, Packaging, Labeling
• 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

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Review

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— Jane DOE, CEO of MyCompany

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