ASQ Inspection Division Webinar (0.1 RU) — Using an Ishikawa Diagram to Identify Special Cause Variation in Control Charts
Webinar Abstract:
Where the results of a process cannot be fully verified by subsequent inspection and testing, the process shall be validated with a high degree of assurance and approved according to established procedures.
However, validation is only the beginning of this requirement. Validated processes must also be controlled and monitored; a requirement generally referred to as continuous process monitoring.
Analyzing a control chart to identify special cause variation can be facilitated by using an Ishikawa diagram
Outline
Where the results of a process cannot be fully verified by subsequent inspection and testing, the process shall be validated with a high degree of assurance and approved according to established procedures.
However, validation is only the beginning of this requirement. Validated processes must also be controlled and monitored; a requirement generally referred to as continuous process monitoring.
Analyzing a control chart to identify special cause variation can be facilitated by using an Ishikawa diagram
Outline
- Discuss continuous process monitoring requirements.
- Identify continuous process monitoring techniques.
- Choose the correct control chart for the type of data.
- Interpret control charts to identify special cause variation.
| Event address for attendees: | https://asq.webex.com/asq/onstage/g.php?MTID=eee2ebcacac679849820cc42c625df58d |
Date & Time
Tuesday May 10th, 2022 6:00pm CDT
End Date & Time
Tuesday May 10th, 2022 7:00pm CDT
Categories
Webinar
Host Type
Technical
Additional Information
Mark Allen Durivage - Managing Principal Consultant
Quality Systems Compliance LLC
Mark Allen Durivage has worked as a practitioner, educator, and consultant. He is Managing Principal Consultant at Quality Systems Compliance LLC, ASQ Fellow, SRE Fellow, and an Expert Faculty Member for AAMI. He holds several certifications including CRE, CQE, CQA, CSQP, CSSBB, RAC (Global), and CTBS. Durivage has written several books available through ASQ Quality Press, published articles in Quality Progress, and is a frequent contributor to Life Science Connect.
Mark primarily works with companies in the FDA regulated industries (medical devices, human tissue, animal tissue, and pharmaceuticals) focusing on quality management system implementation, integration, updates, and training. Additionally, he assists companies by providing internal and external audit support as well as FDA 483 and Warning Letter response and remediation services.
Connect with Mark on LinkedIn: www.linkedin.com/in/markdurivage
Quality Systems Compliance LLC
Mark Allen Durivage has worked as a practitioner, educator, and consultant. He is Managing Principal Consultant at Quality Systems Compliance LLC, ASQ Fellow, SRE Fellow, and an Expert Faculty Member for AAMI. He holds several certifications including CRE, CQE, CQA, CSQP, CSSBB, RAC (Global), and CTBS. Durivage has written several books available through ASQ Quality Press, published articles in Quality Progress, and is a frequent contributor to Life Science Connect.
Mark primarily works with companies in the FDA regulated industries (medical devices, human tissue, animal tissue, and pharmaceuticals) focusing on quality management system implementation, integration, updates, and training. Additionally, he assists companies by providing internal and external audit support as well as FDA 483 and Warning Letter response and remediation services.
Connect with Mark on LinkedIn: www.linkedin.com/in/markdurivage
Event Sponsor Information
ASQ Inspection Division - Monthly Webinar
Add the 2nd Tuesday of each month - 18:00 Central Time Zone - to your Calendar
Inspection Division Events Page: https://my.asq.org/communities/events/158
Add the 2nd Tuesday of each month - 18:00 Central Time Zone - to your Calendar
Inspection Division Events Page: https://my.asq.org/communities/events/158
Category
Public Calendar
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