Unlocking the Power of Root Cause Analysis in Quality Management Systems

Date

May 16 2024

Time

CET Berlin
16:00 - 17:30
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    hours

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    minutes

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Learning Type

Free Live Webinar

Overview

The Good Manufacturing and Good Distribution Practice guidelines expect all departures from the guidelines and a company’s documented QMS to be documented via an investigation. So, what is the difference between an investigation and a good investigation, and what relevance does the Root cause analysis have to an investigation?

An effective RCA process will list all potential causes connected to the deviation/ non-conformance that has occurred. RCA can use several different tools, and some methods may suit the issue at hand better than others. The company’s RCA SOP will guide/ highlight some of the key RCA tools available to understand the root cause of the deviation/ non-conformance.

In this webinar, we will examine what constitutes a good investigation and why it matters so much that we get this right. We will also briefly examine some examples of good and bad RCAs and introduce the appropriate tools and techniques that we would employ depending on the situation/ deviation/non-conformance. Unfortunately, no one-size-fits-all tool exists, and each method has its pros and cons.

All of the above can only be achieved with the correct engagement from the key stakeholders within a company. A good investigation and effective root cause analysis cannot be achieved solely by an individual within a company. This needs to be a collaborative effort, and we will see why this is so important during this webinar.

So join us on May 16th, when we will equip you with tools and scenarios to manage sound investigations and utilise the correct tools to achieve an effective root cause analysis. Thus, you will result in a stronger, more compliant QMS within your companies to prevent recurrences of errors and maximise success!

Don’t miss this exclusive webinar. Register now.

Speaker

  • Kay Flahive
    Kay Flahive
    Contract QP/ QA Consultant

    Kay is a highly experienced consultant QP, Lead auditor and training specialist for Orion GXP Consulting. She has over 30 years of experience in senior Quality and director-level roles in sterile pharmaceutical manufacturing and biotechnology companies in Ireland. This includes a strong analytical background, having worked in QC and validation, as well as operational quality in her more recent QP and Quality systems roles. Kay assists her clients in managing their vendor portfolios and completing QP audits, releasing clinical material and instilling highly effective processes and quality culture in all her roles and assignments.

Partner

Orion GXP Consulting
Orion GXP Consulting
Email
info@oriongxp.com
Website
https://oriongxp.com

Orion GxP Consulting provides contract QP and RP services and consultancy support to pharmaceutical manufacturing and distribution clients, such as training and expert knowledge. Orion GMP Consulting draws on the experience of our consultants and their links to the pharmaceutical industry through consulting and QP/RP roles to assist their clients in developing, managing, and continuously improving their quality systems.

  • Who Should Attend:
    • Head of Quality
    • Head of Regulatory Compliance
    • Compliance Managers
    • QA Managers
    • Regulatory Managers
    • Technical Directors
    • Technical Transfer / NPI Specialists
  • Skill Level: Novice, Intermediate , Expert
  • Topics:

    16:00 – 16:10    Introductions

    16:10 – 16:20 The Background of Good investigation practices

    16:20 – 16:25 What is Root Cause Analysis and why is it important

    16:25 – 15:40 RCA tools 

    15:40 – 15:55 CAPA and linking to Root Cause

    15:55 – 16:10 Summary and questions

  • Special event information:
    • Live attendees will receive a complimentary certificate of attendance.

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Thursday May 2
17:00 - 18:30 Taking risks: ICH Q9 (R1) Quality Risk Management
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Thursday May 16
16:00 - 17:30 Unlocking the Power of Root Cause Analysis in Quality Management Systems
Local Time:
May 16 2024 |
20:00 - 21:30
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If you attend the live session you will get a digital certificate of attendance emailed to you within 7-working days. 

Yes, our event partners will email you the event recording within several weeks. 

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