CAPA for Medical Devices Training that covers CAPA requirements, common root cause investigation tools, and how to prepare for an inspection of the CAPA process.

Our training is for the MedTech Industry including those involved in any part of a CAPA system.

Why Choose Comply Guru?
Highly Interactive, Engaging Experience
Accelerated 'Learn By Doing' Methodology
Delivered by Experienced Practitioners with Proven Expertise
Practical Exercises & Collaborative Learning
Tailored to your Organization
Course Snapshot
 
Approved By
Comply Guru
Duration
16hrs
Teaching Format
Live, Instructor-led Learning
Delivery Options
Virtual or In-Person
Language (s)
English
Price
EUR €  895.00
Learner Rating
★★★★★ 37 Reviews
Upcoming Dates
5th & 6th February 2025 9:00 AM - 5:00 PM GMT
7th & 8th May 2025 9:00 AM - 5:00 PM GMT+1
Why Choose Comply Guru?
Highly Interactive, Engaging Experience
Accelerated 'Learn By Doing' Methodology
Delivered by Experienced Practitioners with Proven Expertise
Practical Exercises & Collaborative Learning
Tailored to your Organization

Upcoming Schedule

Gain a Recognized CAPA Practitioner Qualification

Advance your knowledge and upskill with one of our Instructors.

Secure Payment

Workshop Dates
Daily Schedule
Course Delivery
Location
Fee
Registration
5th & 6th February 2025
9:00 AM - 5:00 PM GMT
2-days Live Workshops
Virtual Workshops
EUR € 895.00
7th & 8th May 2025
9:00 AM - 5:00 PM GMT+1
2-days Live Workshops
Virtual Workshops
EUR € 895.00

Course Structure Explained

Detailed Breakdown & Agenda

Learners first complete interactive eLearning modules to grasp the underlying theory, then attend live, instructor-led workshops emphasizing practical, real-world application.

Time Topic
09:00 - 10:30am

Course Introduction

Practical Workshop The aims of CAPA, Problem-Solving Methods, and Effective Ways to Address Product and Quality Problems

10:30 - 10:45am

Break

10:45am - 12:30pm

Practical Workshop NCR Event vs CAPA

Practical Workshop Scenario Team Based Workshops

12:30 - 1:15pm

Lunch

1:15 - 2:15pm

Practical Workshop Scenario Team Based Workshops, continued

2:15 - 2:20pm

Break

2:20 - 3:30pm
  • Standard Requirements related to CAPA
  • Corrective and Preventive Action Procedure

Practical Workshop, Scenario Team Based Workshops

3:30 - 3:45pm

Break

3:45 - 5:00pm

Practical Workshop Identifying the Problem (Problem Statement – Scenarios)

Daily Wrap Up + Q&A

Time Topic
09:00 - 10:30am

Day 1 Recap

Practical Workshop Identifying the Problem (Problem Statement – Scenarios), continued.

10:30 - 10:45am

Break

10:45 - 11:45am

Practical Workshop Evaluating the Risk and Impact, Determining the Plan to Investigate and Investigating the Problem and determining its Cause

Practical Workshop Create an Action Plan and Implement CAPA Action Plan

11:45am - 12:00pm

Break

12:00 - 1:00pm

Practical Workshop Verify Effectiveness and CAPA Process Steps

1:00 - 1:45pm

Lunch

1:45 - 3:15pm

RCA Methodologies Introduction

Practical Workshop 5 Whys, 8D Root Cause Analysis, Cause & Effect, Pareto Chart

3:15 - 3:30pm

Break

3:30 - 5:00pm

Practical Workshop Root Cause Analysis (5 whys, Fishbone, 8D)

Q&A

Course Survey and Close

Course Overview

CAPA Practitioner

What Will I Learn?

At the end of this course, Learners will have the knowledge & skills to:

  • Understand & implement the Seven CAPA Steps approach.
  • Understand & meet FDA and European expectations when completing CAPAs.
  • Learn how to conduct thorough Investigations into the causes of failure.
  • Identify between Correction and Corrective Action.
  • Identify between Corrective Action and Preventive Action.
  • Generate Corrective Actions that address the Root Causes of failure.
  • Document SMART Effectiveness Checks criteria.
  • Determine the Effectiveness of Corrective Actions.
  • Determine the Overall Effectiveness of a CAPA system.
Who Should Attend?

This course would be targeted at those within the MedTech Industry who are involved in any part of a CAPA system, including:

  • Operators
  • Technical Staff
  • Managers
  • Quality/Regulatory Affairs Personnel
  • Engineering or Support Functions
Will I Get A Certificate?

Successful completion will entitle each Learner to receive a digital Certificate of Completion within 1 business day.

How Will I Be Assessed?

In order to successfully complete this course, each Learner will need to:

  • Maintain 100% attendance and
  • Pass an end of course assessment
What Are The Technology Requirements?

If you are completing this training virtually, the following applies:

There are recommended requirements for each Learner in wishing to complete any of our eLearning modules. In our experience, Workplace IT environments’ internal configurations and available software can vary (new or old), and there may be various limitations or other restrictions in place, and as such, the functionality of any Learning Management System (LMS) may be impacted, restricted and may not perform well. Read the full technology requirements here.

About our Approach to Training

Learn about the benefits and key features of Comply Guru’s Instructor led Learning.

 
Why Choose Instructor led Learning

What Our Learners Are Saying

Read verified reviews from Learners who have completed this course.

Frequently Asked Questions

Yes, we offer in-house training and if you have 5 or more learners that can be trained together, we strongly recommend arranging for in-house training. With this option, there is the possibility of customizing some elements of the training to your organization. Please request a quote and a member of our team will be in touch to discuss this further with you.
We keep our classes to 10 or 12 maximum depending on the blended course, to ensure you can enjoy breakout rooms, activities and Q&As with the Instructor and other participants.
Once you have completed the final assessments, your certificate will be available within 1 business day via your Dashboard. To access your certificate, you must first submit a short course survey and then the certificate will be available for download/print.
Once you have completed the full program, including examination (if applicable), your certificate will be available within 30 business days via your Dashboard once all examination grading has been completed & verified. To access your certificate, you must first submit a short course survey and then the certificate will be available for download/print.
CQI & IRCA Approved Training Provider

CQI & IRCA Approved Training Provider

Offering certified courses since 2019

Exemplar Global Recognized Training Provider

Exemplar Global Recognized Training Provider

Offering certified courses since 2020