Corrective Actions and Continual Improvement Management System

Do you encounter repeating deviations during your operations? This means that the CAPAs set within your organization are ineffective, and the continuous improvement system is lacking. As a result, you have to constantly deal with repeating deviations, wasting time, money, and having stress all the time, because the issues halt the production process.

In this live online interactive and engaging GMP training workshop, you will learn how to process corrective and preventive actions (CAPAs) effectively and maintain an efficient continual improvement system. By the end of it, you will know how to put your organization on the right track towards exceptional effectiveness. You will have much less repeating deviations, and as a result, you will save time, money, improve KPIs and have a stress free working environment,

Date and Time:
21 – 22 September 2021 (4 hours per day + 30 minutes break)
09:00-13:30 CET

Why train alone? Share with collegues:

Share on linkedin
Share on xing
Share on facebook
Share on twitter
Share on email

Reacting to deviations that occur within a process is one thing, but setting practical corrective measures is another. Failing to implement effective corrective and preventive actions (CAPAs) can lead to serious compliance problems. Consequently, it may give regulators a free hand to shut-down your operation without warning. Additionally, not implementing the right CAPAs will lead to repeating deviations will waste time, money, harm KPIs, and cause stress daily.

This course covers the essential elements for managing issues that arise within a product’s lifecycle. It includes the manufacturing, testing, control, and distribution of medicinal products. Also, it provides a best practice framework for managing your reactions to issues that occurred during the life-cycle process.

The workshop will allow you to align yourself with all the requirements of ICH Q10 and ISO 9001:2015 regarding events investigation.

By the end of the workshop, you will know how to create effective CAPAs, which will reduce the number of reoccurring deviations and minimize overdue deviations in the systems. As a result, you will save a lot of time, money, improve KPI’s, and have less stress in your daily routine.


  • CAPA process overview
  • Sources of CAPA and documentation
  • SMART actions
  • Status reporting/rescheduling
  • Effectiveness checks
  • Implementation of a CAPA process

Target Group

This course is for anyone who works within a GMP driven organization and has to initiate or handle CAPAs.

When you deal with CAPAs, you need to make sure they are completed within appropriate timelines to ensure that future issues are prevented. This course is of particular importance to pharmaceutical and medical device quality professionals in all GxP fields

Event Details

The workshop lasts 8 hours and spreads across two days.

17 - 18 February 2021 (4 hours per day), 09:00-13:00 CET


First day of the  2 -day workshop:

Date: September 21, 2021

Start time: 09:00 CET

End time: 13:30 CET

Venue: Virtual



Plus 19% VAT

Limited Spots Available

Your Instructor

Alex Hall

QP Trainer & Consultant

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.

You can learn more about Alex from her appearance on The Qualitalks Podcast:

1. When You Deal With Risk, Don’t Be a Firefighter!

2. The Role of the Qualified Person (QP)

You may also like…

What People Say About Our GMP Online Training

Our online interactive workshops will be presented to you live through a specialized classroom platform. You will be able to attend from home or work, yet feel like we share the same room.

Live Online
GMP Training


See and communicate with the tutor through a webcam and chat


Raise your virtual hand to ask questions


Partake in polls and quizzes


Participate in exercises with other delegates

Let us Know Your Needs

Please share with us several suitable dates for private training sessions and the number of attendees. We will get back to you with a customized offer as soon as possible. 

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