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Statistical Techniques for Process Validation - Made Easy
Part 2 of 2 Click here for Part 1 »
Completed 10 February 2020. Available as recording.
Note. It is not a requirement to attend both PV webinars.
The goal of these two webinars is demonstrate how valid statistical techniques contribute to Process Validation efforts. The application of valid statistical techniques is encouraged by the US FDA’s Quality System Regulation, cGMP, and ISO Standard 13485 for medical devices. The content reinforces the topics covered in the Process Validation Guidance document endorsed by the Global Harmonization Task Force (GHTF). Emphasis will be placed on best practices for quality systems in industry.
These fast-paced webinars will cover the details of application without the burden of statistical complexity. The presenter’s “keep-it-simple” approach will avoid statistical complexity – participants do not need to have a background in statistics.
While most webinars cover the “What and Why” for a subject, these webinars will also give ideas on the “How To” for valid statistical techniques. This “How To” will cover actual examples of application and discuss methods for writing protocols and reports. The discussion of documentation is especially important for FDA-regulated companies.
You will hear directly from an industry expert on this important topic and you can ask questions and get answers. The presenter has over 20 years of experience helping a broad variety of firms apply statistical tools and techniques .
- Explore valid statistical techniques for Process Validation
- Provide a mapping of tools and techniques to IQ, OQ and PQ activities
- Provide examples of industry best practices in each area
- Discuss options for documentation
- Demonstrate how these tools support regulatory compliance, especially if mandatory or voluntary action is required
Program-at-a-glance - Part 2
- Applying Design of Experiments for OQ
- Sampling Plans for PQ
- Process Control Charts for PQ and Process Monitoring
- Question and Answer Period
Who should attend:
This material will appeal to quality professionals and managers in large and small companies.
Instruction is targeted to: quality engineers, process & manufacturing engineers, regulatory compliance professionals, and members of the leadership team.
There are no prerequisites for these webinars. No background in statistics is necessary. That is the foundation of our "keep-it-simple" approach.
When attending a Key2Compliance® course, you get access to Gate2GMP®, our document library and search tool.
Watch this short video to learn more about what Gate2GMP® offers »
Bring this course in-house?
Are you a group in need of the same training?
Do you wish to customize this course to suit your needs?
If so, running the course in-house is probably the best and most cost effective solution.
Peter Knepell, PhD
President, Peak Quality Services
Recorded 10 February 2020
Price (excl. local VAT):
Recording: 250 Euro
Course handouts (PDF) included
For in-house live webinar, contakt us for an offer.
Download and need of software:
The video file is in MP4 / WMV format and is delivered together with the course handouts (PDF) via the WeTransfer service. You have 7 days to download the files.
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