Good Engineering Practices (GEP) - Client Site
12 Sessions
-Validation Life Cycle-Commissioning& Qualification
-Factory Zones& Facility Design
-Clean room Standard& HVAC Components
-Qualification of HVAC System
-Water Systems- Purified
-Qualification of water systems
-Equipment& Automated and Computerized Systems
-Thermal Mapping& Qualification of Compressed air systems
-Autoclave qualification& Pure Steam
-Tunnels and ovens Qualification
-Process Validation
-Cleaning Validation
Suggested alternatives:
Who should attend ?
You must have 6 months of on-the-job experience in engineering, Quality Assurance, or Production.
Course Topics:
Commissioning& Qualification
Factory Zones& Facility Design
Clean room Standard& HVAC Components
Water Systems
Equipment & Cleaning Validation
Automated& Computerized Systems
Course Objectives:
Upon completion of this course you will be able to :
Define the unique characteristics of utilities and production equipment
Ability to define URS for pharmaceutical utilities& Equipment.
Effectively designing, and maintaining a new or existing systems
Define Validation Master Plans
Number of Sessions:
6 Sessions
Instructors :
Dr. Ahmed Badran
Quality Assurance . validation- CSV supervisor
15+ years Experience in Qualification in pharmaceutic
Osama Adel
Technical Manager
Osama AdelTechnical Manager
15+ years Experience in Qualification in pharmaceutical field,
15+ years Experience in Qualification in pharmaceutical field,
Mohamed Saad Mohamed
Pharma Consultant, VALOR GM
20+ years working in pharmaceutical field, working for different pharmaceutical drug manufacturers
20+ years working in pharmaceutical field, working for different pharmaceutical drug manufacturers
المواصفات Good Engineering Practices (GEP) - Client Site
| Attendance type | Client Site |
| Minimum Experience | Zero |
| Number of Sessions | 5 |
| Accreditation | VALOR |