Process Validation Requirements and Compliance Strategies

Added by compliancetrainings on 2018-05-28

Conference Dates:

Start Date Start Date: 2018-06-15
Last Date Last Day: 2018-06-15
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2018-06-08

Conference Contact Info:

Contact Person Contact Person: Alan
Email Email: [email protected]
Address Address: Online Event, Online Event, Online Event, Canada
Phone Tel: 416-915-4438/ 58

Conference Description:

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
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