CAPA and Root Cause Analysis - EU edition MasterClass

17-18 October, 2023

The attendee will also gain practical experience by applying the tools and skills learned to challenging scenarios.

This comprehensive and interactive online course provides the theory of root cause analysis and CAPA management within the context of clinical research.

17-18 October, 2023, Virtual

Time Zone: UTC/GMT+1/CET

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Key learnings

Appreciation

Appreciation of the critical role of root cause analysis and CAPAs and their relationship to risk management within the Quality Management System

Understanding

A thorough understanding of the standard methods of root cause analysis

Practice

Practice conducting effective root cause analysis using scenarios

Skills

The skills to implement effective CAPAs to prevent the recurrence of errors and non-compliances

CAPA

Practice in creating effective CAPAs using scenarios

Templates

Templates and tools to adapt for use beyond the course

Trusted by over 17,000 delegates across leading companies

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Overview

masterclass in pharma img

Overview

This comprehensive and interactive online course provides the theory of root cause analysis and CAPA management within the context of clinical research. The attendee will also gain practical experience by applying the tools and skills learned to challenging scenarios.

#masterclass #glceurope #pharma #globaltraining #CAPA #rootcauseanalysis

Trainer

Claire Noble

Claire has worked in pharma and healthcare for more than 30 years in the NHS, home healthcare, clinical trial supplies, and quality compliance for clinical operations at the global and UK level for a major global pharma company. She has an MSc (Cran) in Quality Management in Scientific Research and Development and currently works as a freelance specialist combining her areas of passion: GCP, training, and leadership skills.

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Reasons to attend a masterclass

Practical knowledge

Venture into undiscovered territories and gain inspiration through collaboration

Interactivity

Boost your professional skills by directly engaging with domain experts

World-class trainers

Gain value and learn from the best instructors

Networking

Build a top-notch community and advance your career

Who should attend img RECOMMENDATION

Who should attend?

• QA/QC
• Regulatory, safety, study managers
• Investigational site staff
• Clinical Research Associates (CRA)
• All roles within clinical research involved in:
• Investigations into process failures, non-compliances, errors and the actions required to prevent them recurring
• Developing responses to regulatory inspection or audit findings

Ticket options for you

Full event
pass

Team participation?

*minimum of 10 participants

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Testimonial

Our success stories

"High attention to detail in course content and very well delivered"

Simon Halsey

Product Development Manager
Essentra Packaging
United Kingdom

Our success stories

"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"

Aurelie Vivicorsi

USP PD Team Manager
Celonic AG
Switzerland

Our success stories

"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"

Emilia Szwej

Manager, Senior Investigator
MT Sword Laboratories (BMS)
Germany

About GLC

Global Leadership Conferences began as an ambitious dream by three founders ten years ago. Today it’s an international series of interactive events, exploring the hottest topics in critical fields. Each year, thousands of professionals join us to challenge the status quo and learn innovative ways to create new solutions in Finance, Pharmaceutical, HR, Health & Safety, and Energy.

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Speakers

17,761

Attendees

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