Overview:
This Process Validation Requirements webinar will review process validation basics, with emphasis on looking beyond compliance towards achieving a robust process. Review of process validation basics, with emphasis on looking beyond compliance towards achieving a robust process.
Why should you Attend: When used as intended, process validation can provide increased process reliability, improved yields, and reduced operating expenses.
Areas Covered in the Session:
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
This Process Validation Requirements webinar will review process validation basics, with emphasis on looking beyond compliance towards achieving a robust process. Review of process validation basics, with emphasis on looking beyond compliance towards achieving a robust process.
Why should you Attend: When used as intended, process validation can provide increased process reliability, improved yields, and reduced operating expenses.
Areas Covered in the Session:
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
Speakers
Jose Mora,
Who Should Attend
- 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
- Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
