![Good Manufacturing Practices [cGMP]](/web/image/product.product/2191/image_1024/Good%20Manufacturing%20Practices%20%5BcGMP%5D%20%28In-person-%20Virtual%29?unique=3b34d6a)
Good Manufacturing Practices [cGMP]
Course Topics: (7 Modules)
1. Quality Systems (2 Sessions)
2. Laboratory System (2 Sessions)
3. Infrastructure: Facilities, Utilities, Equipment (2 Sessions)
4. Materials management (1 Sessions)
5. Manufacturing Systems (1 Sessions)
6. Filling, Packaging, Labeling (1 Sessions)
7. Product Development (1 Sessions)
Number of Sessions:
10 Sessions
Suggested alternatives:
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:
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 ( QMS, GDP, Deviation management, Change control, supplier qualification, APR)
• Laboratory Systems ( Compendia, Specifications, Sampling, record-keeping, Instrument handling, Stability programs, OOS)
• Infrastructure: Facilities, Utilities, Equipment
• Materials & Distribution management
• Manufacturing , Filling, Packaging& Labeling Systems
• Product Development
Number of Sessions :
10 Sessions
Instructor:
SPEAKER
Dr. Nabil Mofeed
Senior Supervisor of R&D stability labs.
+11 years experiences in quality control, master degree in analytical chemistry
+11 years experiences in quality control, master degree in analytical chemistry
Speaker
Eman Salah
Compliance Section Head
+12 years of experience in pharmaceutical Quality Systems, TQM, Master's degree, Pharmaceutics
SPEAKER
Dr. Mohamed Saad
Pharma consultant, VALOR GM
+20 years working in pharmaceutical field, working for different pharmaceutical drug manufacturers, VALOR co- founder
SPEAKER
Dr.Akram Bashir
Branch Manager of Nawah Scientific and the formulation Lab.
15+ years working in pharmaceutical R&D field, working at different pharmaceutical drug manufacturers
Specifications for Good Manufacturing Practices [cGMP]
| Attendance type | In-person/ Virtual or E- Learning |
| Minimum Experience | Zero |
| Number of Sessions | 10 |
| Accreditation | VALOR |