Key Topics

In this webinar, you will learn the best practice framework for deviation investigations. Additionally, you will familiarize yourself with an approach you can apply to all relevant product life-cycle. 

Investigation Process

Correct Documentation of Deviations

Impact / Risk assessment

Best Practices of Investigations

CAPAs & Follow up​

Speaker

Alex Hall

Alex is an expert in Pharmaceutical Quality Assurance with 30 plus years in the pharma industry, 20 of those as a Qualified Person.

As an instructor, Alex builds on her experience and her previous role as a UK QP Assessor to support QA professionals and QP trainees. She helps trainees achieve the best results through supportive coaching, mentoring, and a straightforward training approach.

Visit Alex on LinkedIn.  

Do you want to learn more about handling deviations and CAPAs effectively? 
Join us at our online workshop, Deviations, and Issue Management Systems.

In this 9-hour workshop, you will master the essential elements for investigating deviations that arise during medicinal products’ product life cycle and learn how to document and address deviations much more effectively.

At the end of the 2-day session, you will know how to reduce the reoccurrence of deviations in your organization and minimize overdue issues in the QMS.

As a result, you will boost your compliance, improve KPI, and save much time and money in the process.
Besides, fewer deviations mean less stress at the workplace and a much healthier business environment.

Wait, don't leave empty-handed!​

Download our free Ultimate FMEA Guide, which is dedicated to GMP and pharma professionals.

This extensive yet simplified guide to Failure Mode and Effects Analysis (FMEA) will help you master one of the most vital instruments in your risk management toolbox.

Get Informed About

Free Webinars
Industry Insights
New Workshops
Special OFFERS

Subscribe now

.