ComplianceOnline

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

Instructor: Vinny Sastri
Product ID: 701124

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

$500.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556

Email: customercare@complianceonline.com

Read Frequently Asked Questions

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.

Description

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

Instructor Profile
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.

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