Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies

This Process Validation training will detail the key qualification steps in process validation, the use of statistical methodology for sampling plans and acceptance criteria, how to handle deviations, elements of a good validation summary report. Process validation is critical to the production of high quality, consistent, safe and effective products and devices. Routine end-product testing alone is insufficient to assure the quality, safety and effectiveness of a product or device. It is important that the product acceptance criteria and specifications are quantified, and that the manufacturing processes are well characterized, understood, controlled and validated.

Part 2 in this two-part series will detail the key qualification steps in process validation, the use of statistical methodology for sampling plans and acceptance criteria, how to handle deviations, elements of a good validation summary report, change controls and revalidation. Sustainability and maintaining a validated state will also be discussed.

Areas Covered in the seminar:

• Process validation Planning and Prerequisites - recap from Part 1.
• Installation Qualification (IQ).
• Operational Qualification (OQ).
• Performance Qualification (PQ).
• Statistical tools, techniques and quality metrics.
• Sampling Plans.
• Process Control.
• Deviations and how to handle them.
• Validation summary reports.
• Change Controls.
• Revalidation.
• Validation Life Cycle.
• Click Here for Module 1 detailed description

Who Will Benefit:

• This Webinar will be of value to all those involved in product development, process development, quality control, quality assurance, and manufacturing
• Research and Development personnel
• Product development personnel
• Process engineers
• Manufacturing managers and engineers
• Validation Managers and Engineers
• QA/QC managers and personnel
• Regulatory personnel
• Project managers