This training is intended to help you better understand and get familiar with best practices for Process Validation applicable for the highly regulated biological/pharmaceutical industry. This course is further intended to discuss the life cycle of the Process Validation system. You will learn when a process should be validated, the basic components of a Process Validation and how to write protocols and reports.
Who should attend ?
This training was developed for professionals engaged within a variety of processing industries, including Pharmaceuticals, Biopharmaceuticals, Biotechnologies, Cosmetics, Chemical and Specialty Chemicals.
The tools in this course will be very beneficial for
Quality Control Professionals.
and anyone whose’ s job requires product and manufacturing processes design, optimization, troubleshooting, etc.
•Life Cycle Approach of Process Validation
•Phase 1 : Process Design - Case Study
•Phase 2 : Process Performance Qualification (PPQ)
•Phase 3 : Continued Process Verification (CPV)
•Workshop : Creation of protocols for solid , Liquid, and Semi_ Solid products.
Number of Sessions :
Mohamed El- Khatieb
Head Of Quality Assurance
14+yearsof qualitysystem experience -Speaker at PHARMACONEX Conference - ASQ Certified Six Sigma Black Belt
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