Quality Assurance professionals play a pivotal role in ensuring compliance with standard operating procedures and regulatory requirements. However, merely addressing deviations is insufficient without a robust strategy to prevent their recurrence. Identifying and addressing the underlying root causes is paramount to establishing a resilient quality management system. This workshop goes beyond surface-level analysis and embraces a holistic approach to process improvement.
<p.By leveraging Lean principles, participants will explore innovative methods for root cause identification that transcend conventional attributions such as "human error." The tools and techniques presented in this workshop empower attendees to streamline processes and minimize deviations, ultimately enhancing operational efficiency and regulatory compliance.Join us to gain actionable insights that can be immediately applied to your daily work, simplifying processes and reducing the time and effort required to complete tasks. Elevate your CAPA strategy and drive continuous improvement within your organization.
This workshop is tailored for Quality Assurance professionals, internal auditors, and individuals involved in regulatory compliance across various industries. It is also beneficial for those seeking to deepen their understanding of CAPA principles and best practices, especially within pharmaceutical, biotechnology, and medical device sectors.
Understanding Lean Principles:
Explore how Lean principles, such as waste reduction and continuous improvement, are applicable to CAPA processes, enhancing efficiency and effectiveness.
Problem Definition and Root Cause Identification:
Develop essential skills in articulating and defining problems within CAPA processes, alongside proficiency in identifying underlying root causes, fostering targeted and efficient problem-solving.
Lean Problem-Solving Mastery:
Acquire expertise in Lean problem-solving methodologies, enabling systematic approaches to address deviations within CAPA processes, driving continuous improvement and quality enhancement.
Corrective Action Application and Verification:
Apply Lean principles to develop robust corrective actions aimed at addressing identified root causes, ensuring effectiveness through verification and ongoing monitoring of results within CAPA workflows.
All participants will receive a certificate of attendance upon completion of the workshop.
Note: Registration closes one week prior to the start of workshop. Workshop registration is intended for individual use only. Each registration grants access to one participant. If you plan to attend as a group or company team, please ensure that each participant is registered separately. Group rates and corporate packages are available—contact us for details.
Refunds are only available if cancellation is requested at least 48 hours before the workshop. No refunds will be issued for late cancellations.

AAPS Instructor
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AAPS Instructor
Ms. Pilkey has been involved in the pharmaceutical industry at both the government and private level for 44 years. She was involved in performing GMP and Medical Device inspections with the Health Products Food Branch Inspectorate of Health Canada. She has also performed chemical analyses both with Health Canada and Industry.
She has recently retired from her position as the Regulatory Affairs Director at Eurofins Biopharma Product Testing Toronto, Inc. where she served as a Regulatory/Quality Control consultant and auditor to clients who are involved in fabrication, packaging, testing, importation, distribution, and wholesaling Drug Products, Natural Health Products, Medical Devices, and Medicinal Cannabis.
Currently, she serves as an executive member and Quality & Compliance Department Head at AAPS Pharma
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