Best Practices for Deviation Training

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Speaker : DANIELLE DELUCY
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When : Wednesday, August 18, 2021
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Time : 01 : 00 PM EST
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Danielle DeLucy, MS, is the owner of ASA Training and
Consulting, LLC which provides Pharmaceutical and Biologics based
companies with training and quality systems assistance in order to meet
regulatory compliance. Prior to this role, Danielle has been in the
industry for 15 years serving in numerous Quality Management Roles, such
as the Director of Product Quality, the oversight of Sterility
Assurance practices, and provided QA oversight of numerous filling and
packaging operations. Danielle began her QA career as a Quality Control
Pharmaceutical Microbiologist at a contract laboratory where she
performed various tests for their clients. In the years after, she has
held positions in the Quality management arena while increasing her
responsibility. She has helped to lead many Regulatory Health
Inspections and was instrumental in the coaching process of her peers
prior to any inspection. Currently, Danielle assists companies who are
faced with warning letters, consent decrees, and those wishing to
improve compliance to establish more robust quality systems so that the
company can succeed.
Deviation investigations are a very common topic to be reviewed during FDA investigations. Ensuring the firm has robust and complete write-ups of these situations is key to a successful audit. Having inadequate investigations could potentially cause some severe issues for the company and may sometimes result in warning letters, consent decrees or recalls.
Learning Objectives
- Discuss what to do when problems occur
- Outline the requirements of the Deviation and procedure including the deviation report
- Choose the most appropriate Root Cause Analysis methods for the situation
- Discuss how to conduct the deviation and the tools to be used in the process
Areas Covered
- Review of FDA and Regulatory Requirements for Investigations
- What is the definition of a Deviation?
- Types of Deviations/Identification of Deviations
- Conducting the Investigation
- Interviews – dos and don’ts
- Source Documents/Evidence
- Determining Root Cause and Effective/Sustainable CAPA to avoid 483 observations
- Key Elements of the Investigation Report
Course Level - Basic
Who Should Attend
- Site Quality Operations Managers
- Quality Assurance Personnel
- Plant Managers and Supervisors
- Manufacturing Superintendents and Managers
- Regulatory Affairs Managers
- QC Lab staff
Why Should You Attend
This
webinar will help attendees understand the fundamental steps of a
deviation investigation with a focus on using facts and objective
evidence to arrive at root cause and CAPA. This webinar will focus on
how to avoid the pitfalls that may occur during FDA inspections and help
eliminate 483 observations. Learn how to identify and avoid potential
pitfalls during deviation investigations.
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$179.00
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