This webinar on Process Validation Requirements will go over the foundations of process validation, with an emphasis on going beyond compliance to achieve a robust process. Review of the fundamentals of process validation, with an emphasis on looking beyond compliance to achieve a robust process.
Why Should You Attend:
When applied correctly, process validation can result in higher process dependability, higher yields, and lower operating costs.Areas Covered in the Webinar:
- Global Harmonization Task Force requirements (includes FDA and ISO)
- Installation Qualification (IQ)
- Operational Qualification (OQ)
- Performance Qualification (PQ)
- Design Qualification
- Facilities and utilities
- Strategies for achieving a robust and reliable process.
- Typical process validation protocols.
Who Will Benefit:
Managers, Supervisors, Directors, and Vice-Presidents in the areas of:- Research & Development
- Quality Engineers and Auditors
- Manufacturing Engineers
- Quality Assurance & Quality Control Teams
- Operations Teams
- Document Control
- Device Development Teams
- Personnel involved in Verification and Validation planning, execution and documentation for devices
- From Pharmaceutical, Medical Devices, Biotechnology, Clinical Trial and Clinical Research Companies
Course Provider
Jose Mora,
