Quality Event Management and the CAPA System Part 1: Using a Closed-Looped System
In this webinar series, learn how to improve your company’s corrective and preventive action (CAPA) process by employing a closed-loop system. MasterControl Partner Ken Peterson explains how a three-loop approach to quality event management (QEM) helps you avoid death by CAPA by focusing your efforts on the most critical areas.
When companies indiscriminately take every quality event through the CAPA process, the quality department becomes overwhelmed, leading to quick fixes that don’t always get to the root cause of a problem. By using a risk-based approach, companies can quickly resolve less important issues and spend most of their resources on critical quality events.
Ken Peterson walks viewers through the risk-based review process, including the critical thinking to ultimately get to the root cause of a problem. He presents steps that will work in any industry, for any problem. Learn how to get all the information you need to correct a quality event and remain compliant.
Learn more about CAPA management on our website https://www.mastercontrol.com/capa-software/capa/?utm_campaign=7013x000001y6ZMAAY&utm_medium=PR-AR-Social&utm_source=YT
Watch part two of the series here https://www.youtube.com/watch?v=AVnegiEMK4w
Learn why the future of quality is directly related to data https://www.mastercontrol.com/library/ultimate-guide/data-driven-quality/?utm_campaign=7013x000002dfbFAAQ&utm_medium=PR-AR-Social&utm_source=YT
Learn about the hidden costs of quality in our white paper https://www.mastercontrol.com/library/white-papers/digital-data-operational-efficiency/?utm_campaign=7013x000002dfbAAAQ&utm_medium=PR-AR-Social&utm_source=YT
Subscribe for more informative content http://bit.ly/2RZAtKa
MasterControl Inc. is a leading provider of cloud-based quality and compliance software for life sciences and other regulated industries. Our mission is the same as that of our customers – to bring life-changing products to more people sooner. The MasterControl Platform helps organizations digitize, automate and connect quality and compliance processes across the regulated product development life cycle. Over 1,000 companies worldwide rely on MasterControl solutions to achieve new levels of operational excellence across product development, clinical trials, regulatory affairs, quality management, supply chain, manufacturing and postmarket surveillance. For more information, visit https://www.mastercontrol.com/?utm_campaign=7013x000002dfbAAAQ&utm_medium=PR-AR-Social&utm_source=YT
Видео Quality Event Management and the CAPA System Part 1: Using a Closed-Looped System канала MasterControl
When companies indiscriminately take every quality event through the CAPA process, the quality department becomes overwhelmed, leading to quick fixes that don’t always get to the root cause of a problem. By using a risk-based approach, companies can quickly resolve less important issues and spend most of their resources on critical quality events.
Ken Peterson walks viewers through the risk-based review process, including the critical thinking to ultimately get to the root cause of a problem. He presents steps that will work in any industry, for any problem. Learn how to get all the information you need to correct a quality event and remain compliant.
Learn more about CAPA management on our website https://www.mastercontrol.com/capa-software/capa/?utm_campaign=7013x000001y6ZMAAY&utm_medium=PR-AR-Social&utm_source=YT
Watch part two of the series here https://www.youtube.com/watch?v=AVnegiEMK4w
Learn why the future of quality is directly related to data https://www.mastercontrol.com/library/ultimate-guide/data-driven-quality/?utm_campaign=7013x000002dfbFAAQ&utm_medium=PR-AR-Social&utm_source=YT
Learn about the hidden costs of quality in our white paper https://www.mastercontrol.com/library/white-papers/digital-data-operational-efficiency/?utm_campaign=7013x000002dfbAAAQ&utm_medium=PR-AR-Social&utm_source=YT
Subscribe for more informative content http://bit.ly/2RZAtKa
MasterControl Inc. is a leading provider of cloud-based quality and compliance software for life sciences and other regulated industries. Our mission is the same as that of our customers – to bring life-changing products to more people sooner. The MasterControl Platform helps organizations digitize, automate and connect quality and compliance processes across the regulated product development life cycle. Over 1,000 companies worldwide rely on MasterControl solutions to achieve new levels of operational excellence across product development, clinical trials, regulatory affairs, quality management, supply chain, manufacturing and postmarket surveillance. For more information, visit https://www.mastercontrol.com/?utm_campaign=7013x000002dfbAAAQ&utm_medium=PR-AR-Social&utm_source=YT
Видео Quality Event Management and the CAPA System Part 1: Using a Closed-Looped System канала MasterControl
Показать
Комментарии отсутствуют
Информация о видео
Другие видео канала
MasterControl Quality Management System (QMS) DemoHow to estimate risk for a medical device according to ISO 14971:2019Supply Chain Management and Importance of People | Chethan Kote | TEDxUniversityofStrathclydeQuality by DesignMANAGER Interview Questions and Answers! (How to PASS a Management Job Interview!)ISO 9001 IN A NUTSHELL | How it Works and How it Can Work For YouWarehousing - 10 Principles of Design and OperationsQuality Event Management and the CAPA System Part 3: Effectiveness Checking20 Ideas for Managing CAPA and the Inspectional ProcessRoot Cause Analysis Course - 5 Whys and Fishbone DiagramOracle NetSuite ERP Implementation Challenges Revealed [Common Risks and Pitfalls]5 Things the Audit Committee Won't Tell Internal AuditISO 9001:2015 PDF CHECKLIST | PDF Guide to ISO 9001 Quality Management Systems7 SENIOR MANAGER / DIRECTOR Interview Questions and Answers!Beginning Engineers PPAPManagement of an Effective CAPAQuality Improvement in HealthcareISO Internal Quality Audit (IQA) Explained‘Corrective Action’ VS ‘Preventive Action’ (CAPA) -HindiCorrective and Preventive Action (CAPA) 820.100 & ISO 13485 § 8.4 & 8.5 (Executive Series #45)