11/16/2021
Date: 27 January 2022
Time: 10:30 AM - 12:00 PM EST
Location: Interactive Webinar
Registration: HERE
Cost: AGXPE Member – $79.00
Non-Member Registration – $89.00
The Association for GXP Excellence (AGXPE) will host the 90-minute interactive webinar led by Sam Sather and Keith Dorricott, founders of DIGR-ACT®. This session will address the challenges in using root cause analysis (RCA) to lead to effective risk assessment and Corrective and Preventive Actions (CAPA) for GXP.
Training on RCA does not usually happen, so many do not know how to carry out a proper RCA. Yet, it is an important step in understanding what happened so the issue(s) can be prevented from recurring. In this webinar, you will learn about a practical approach to RCA that shows results while encouraging critical thinking for GXP professionals.
These sessions introduce the GXP audience to DIGR-ACT® as a solution to mature teams and processes in the era of big change. Attendance at this or another session (live or recorded) is required before attending the Train-the-Trainer workshop scheduled for February 15 & 22.
Refer to the February Train-the-Trainer sessions HERE for more information and to sign-up; space is LIMITED.
Session Objectives:
Describe how critical thinking is needed and implemented for managing risks and issues that matter.
Recognize the limitations of current approaches to risk and issue management, and what is needed to support the maturity of the organizations’ teams.
Learn the components of a new approach that supports critical thinking to focus on Critical to Quality Factors.
Learn more about DIGR-ACT® with Clinical Pathway’s blog series! The following two you may find interesting, with more to read in our blog series.
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About the Presenters:
Sandra “SAM” Sather
Clinical Pathways
samsather@clinicalpathwaysresearch.com
Sandra "SAM" Sather’s current focus of consulting is to promote clinical quality systems for Sponsors/CROs and Investigators/Research Institutions. She has over 35 years of clinical experience, has a Bachelor of Science degree in Nursing and a Master of Science degree in Education with a Specialization in Training and Performance Improvement. SAM has been dual certified by the Association for Clinical Research Professionals (ACRP) for over 15 years as a CCRA and CCRC. She is a current ACRP Fellow, which is awarded to individuals who have made substantial contributions to the Association and the industry at large. She is a frequent speaker at industry conferences and has authored dozens of courses for clinical research training programs in various functional areas. She has multiple training, monitoring and project management experiences of diverse size, and objectives with a variety of global clients. In 2002 she co-founded Clinical Pathways (CP), LLC with Charles "Chuck" Sather.
Keith Dorricott
Dorricott Metrics & Process Improvement Ltd.
keith@dorricottmpi.com
Keith Dorricott is the Director of Dorricott Metrics & Process Improvement Ltd., formed in 2016. Over a 12 year period, he worked in R&D, process development, and manufacturing whilst at Kodak Ltd. In 2005 he moved industry into the area of clinical trials and worked for two major CROs leading corporate process improvement. He qualified as a Black Belt in Six Sigma in 2002 and a Master Black Belt in Lean Sigma in 2007. He is an Ambassador for the Metrics Champion Consortium (MCC) and assists by facilitating work groups on centralized monitoring, central lab metrics, vendor oversight, Trial Master File, and by developing tools to assist with risk assessment & control and metrics selection & use. He received the MCC Champion Award in 2016 for making significant contributions to advancing the MCC mission to improve the efficiency, quality and effectiveness of clinical trials. Keith regularly presents at conferences such as DIA and SCOPE on the practicalities of quality risk management and risk-based monitoring and the definition and use of metrics. His passion is to help bring clinical research to the proficiency of manufacturing with root cause analysis skills – a fundamental requirement for effective process improvement.
- The Clinical Pathways Team
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