Description
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
R&D Scientists.
Quality Control Professionals.
Quality Assurance
Production Professionals
and anyone whose’ s job requires product and manufacturing processes design, optimization, troubleshooting, etc.
Key Takeaways
- Flexible Attendance Options – Join in-person at VALOR or virtually through our live interactive platform.
- Recorded Sessions – Enjoy limited access to recordings for one month after course completion for review and reinforcement.
- Repeat for Free – Participants may re-attend inperson any future round of the same course at no additional cost.
- Accredited Certificate – Receive a QR-coded certificate for authenticity verification and professional recognition.
- Comprehensive Resources – Access digital materials, trainer support, and post-course assessments through VALOR’s e-learning platform
Course Topics
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 product
Workshop : Creation of protocols for Liquid/ Semisolid product
Workshop : Creation of protocols for Parentral product
Number of Sessions
4 Sessions