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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.
- Validation Life Cycle.
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
Dr. Vinny Sastri, President of WINOVIA® LLC, and has over 20 years experience in new product development and quality improvement with a strong track record in the healthcare, medical device, electronics and consumer goods industries. He is a certified Six Sigma blackbelt. Winovia LLC a consulting company that provides sustainable solutions new product development, quality improvement and high performance materials with the goal of strategic market penetration, improving efficiencies of products, processes and services, streamlining business processes, reducing operational costs, improving margins and increasing revenues and profits for its clients.
ComplianceOnline would process/provide refund only if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs."
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