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Sunday June 15, 2025 9:00am - 5:00pm EDT
TBD
Component Type: Tutorial
CE: ACPE 6.50 Application UAN: 0286-0000-25-508-L04-P; CME 6.50; RN 6.50

Pre-registration required and is an additional fee. *Please note: Short Courses are stand-alone events. Registration for the main conference, forum, etc. are not mandatory. Already registered? Log in to DIA's My Account/ My Events. According to the FDA (as well as other regulators), corrective and preventive action (CAPA) management and lack of proper investigation of challenges is a top observation among companies in the industry. In this short course, through interactive case studies, participants will learn how to conduct a proper investigation into a robust root cause analysis using industry standard tools in a toolkit approach. Additionally, participants will explore the challenges of proper CAPA planning and define appropriate effectiveness checks to ensure these observations do not occur again and how to properly document what was performed. Real-life case studies from various FDA 483s will be explored to showcase how to apply our toolkit approach to avoid action by regulators and ensure compliance in your processes and company culture. Receive $50 off your Global Annual Meeting total purchase by registering for two or more Short Courses. Purchases must be made at the same time to receive the discount. Discounts will be reflected on the last page of the cart.

Who should attend?

Professionals who want a better understanding of how to perform a robust root cause analysis and CAPA plan to shift from a reactive organization to a proactive organization. This workshop is best suited for those in regulated industries in various industry areas such as quality, regulatory, operations/production, laboratories, etc.

Learning Objectives

  • Determine the best approach to train individuals on industry best practices in CAPA management
  • Utilize proven tools, in a toolkit format, to properly investigate observations and formulate robust CAPA plans and effectiveness checks to ensure compliance and remediation of observations
  • Analyze case studies for techniques and strategies that will help solidify how to use the different tools


Speakers
avatar for Brendan Burns

Brendan Burns

Manager, Document Control & Training, Mersana Therapeutics, United States
Brendan is a Manager, Document Control & Training at Mersana Therapeutics, with over 15 years of biopharma industry experience in development landscapes ranging from preclinical to commercial organizations. Overall background includes roles ranging from manufacturing operator on the... Read More →
avatar for Christy Mazzarisi

Christy Mazzarisi

Quality and Clinical COE Lead, Network Partners Group, United States
Head of Quality, with a broad background in Pharmaceutical and Laboratory sciences (specializing in business development) with R&D and commercial manufacturing (sterile and non-sterile) experience with over 17 years industry practice. Overall background and specialties include GMP... Read More →
avatar for Danielle Metzger

Danielle Metzger

Principal Quality Consultant, PharmaQ Consulting, United States
Accomplished Quality Professional with a broad background in pharmaceutical life sciences having R&D through commercial experience with 25 years of practice in Quality & Manufacturing, global consulting, and business development. Experienced and well versed in GMP and have working... Read More →
Sunday June 15, 2025 9:00am - 5:00pm EDT
TBD Walter E. Washington Convention Center 801 Allen Y. Lew Place, NW Washington, DC 20001-3614 USA
  08: RD-Quality-Compliance, Tutorial |   20: Short-Courses, Tutorial
  • format csv
  • Credit Type ACPE, CME, RN
  • Tags Tutorial

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