Process Validation Requirements & Compliance Strategies

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