Process Validation Requirements and Compliance Strategies

Date	Jul 16, 2019
Time	12:00 PM EDT
Cost	$200
Online

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. 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

Who Should Attend:

• Research and Development Departments
• Engineering Departments
• Quality Departments
• Manufacturing Departments
• Operations Departments
• Production Departments
• Document Control Professionals
• Device Development Teams
• Quality Auditors
• Personnel involved in Verification and Validation planning, execution and documentation for devices

MD3046