Good Clinical Practice
for Advanced Therapy Medicinal Products

Refresher based on ICH E6(R3)

DIGITAL TRAINING COURSE

Your Course

For Clinical Trial Professionals working with Cell and Gene Therapies who need to stay compliant with evolving GCP standards and ATMP guidelines.


With the GCP for ATMPs Refresher based on ICH E6(R3), you can ensure inspection-readiness and regulatory compliance – despite the complexity of ATMP development.   Achieve GCP compliance without wasting time on generic training or missing ATMP-specific nuances.

Your Situation

You’re constantly navigating complex ATMP regulations and want more clarity and confidence...

… but GCP updates and ATMP-specific requirements are holding you back.

You want to ensure inspection-readiness... 

… but limited time and generic GCP courses leave you unprepared.

You want to Get Trained on all GCP Updates ... 

... but you don't know How to Prioritize and Make your Day more Efficient.

You’re striving to improve your clinical trial oversight and documentation...

… but you feel overwhelmed by regulatory ambiguity.

Your Learning Objectives

How about you would be able to apply the updated GCP Principles to your Clinical Trials with Cell and Gene Therapies?
It just takes 1 day time.
  • Define your Priorities with a Risk-based Approach and manage them effectively, resulting in less Stress and Overload.
  • Schedule 1 Hour per Day into your calendar to complete the course in your own pace, keeping track of your Daily Business.
  • Invest your Time with a tailored approach that you can ensure you have enough time for your Tasks.
  • Use the learned Concepts so that you feel Productive and Energized throughout the day instead of being exhausted in the afternoon.

You too can achieve GCP Confidence
in ATMP Clinical Trials –
without wasting Time on generic Training.

My Promise to You
Never again feel unsure about GCP compliance in ATMP Clinical Trials.
You’ll gain the tools and confidence to lead your clinical trials with Regulatory Compliance and Clinical Excellence.
You don’t think that’s possible when you look at your current uncertainty around ATMP-specific GCP?

I understand.
Many professionals I’ve worked with felt the same way—overwhelmed by evolving regulations, unsure how to apply ICH E6(R3) in the context of ATMPs, and frustrated by generic GCP trainings that didn’t address their real-world challenges.
I was there too—until I started breaking down the ICH guidelines into practical, ATMP-relevant modules and developed a method that combines:
• Scientific accuracy from the ICH E6(R3) guideline,
• Hands-on experience from 15+ years in clinical operations,
• And real-world tools like checklists, summaries, and inspection prep guides.

This is exactly what I now present to you - on a silver platter - so you don’t have to figure it out alone. If I could assure you that this course will give you clarity, confidence, and compliance - Would you be ready to take the next step?

Understand the lastest GCP Updates & ATMP Guidelines

Get a Comprehensive Overview of the updated GCP with ICH E6(R3) plus most relevant ATMP Guidelines.

Enhance Oversight for ATMP Clinical Trials


Implement Risk-Based Sponsor Oversight and Focus on the Critical Aspects of ATMP Clinical Trials.

Avoid Inspection Findings


Apply the Practical Learnings to your Daily Business and achieve Patient Safety and Data Integrity.

Your Time Investment

  • Over 4,5 hours of Videos and Presentations
  • Over 1 hour of Practical Exercises
  • Around 10 min Quiz after each Module
  • Roughly 2 min Learning Diary after each Module

Your Trainer

Hello, it’s me, Jessica Cordes, a Clinical Operations Enthusiast.

Throughout my 15-year journey in clinical drug development, I've been captivated by a complex clinical trial environment, particularly in addressing the critical needs of patients battling blood cancer and solid tumors.
In my leadership roles within Clinical Operations over the past 6 years, I've cherished the collaborative spirit that fueled our pursuit of innovative cell and gene therapies, an environment with even more regulatory requirements.
Witnessing the convergence of expertise and empathy, I didn't just develop drugs; I worked with truly inspiring and cohesive teams.

Since many years I am enjoying to give my experience and knowledge to the industry; trying to make a difference to the usually boring GCP trainings.

Jessica Cordes

Senior Consultant | Trainer

Your Benefits

1 - Efficient & Flexible

You have the opportunity for a Self-Directed Learning. You can progress at Your Own Pace without being tied to fixed training times.

Compared to traditional classroom training, you Save Time and Travel Costs.

2 - Updated & Relevant

You learn based on the Updated GCP Guideline and ATMP Guidelines.
You train with Practical Exercises the application of GCP in Real-World Scenarios.

3 - Interactive

The exercises come along with different Types of Interaction to give you a Learning Experience.
Additionally, you can Connect to other Learners via a Community.

4 - Certified

After each module you comple a Quiz.
At the end of the course, you will receive a Training Certification.

Your Course Agenda

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Your Guarantee

You will receive a training certificate that is compliant with inspector's expectations.
Updates
The course content is regularly updated to reflect the latest developments, including the Declaration of Helsinki (2024) and ICH E6(R3) (2025), as well as the most relevant ATMP Guidelines as of June 2025.

Frequently asked Questions

How much time do I need to plan for the course?

Overall, please plan approximately 6 hours to complete this course.
You can complete it in one go or in short sessions.
If you only take about  72 minutes of your time each day, you can complete the course within 1 week, without deprioritizing your daily tasks.
You can stop and continue the course whenever you want.

Is the GCP for ATMPs Refresher worth it?

Absolutely. This course is tailored to Cell and Gene Therapies – no fluff, just what you need.
You get a self-directed learning experience and can progress on your own pace. You learn the GCP updates according to ICH E6(R3) not only frontal but train your learnings with real-world scenarios. Beside the interactive learning you are able to connect to your peer learners via the Clinical Excellence Training Academy (CE-T-A) Community.

I doubt that the course will not be boring. How can I be sure?

It's natural to be skeptical. You've probably already done many boring online trainings. Me, too.
My GCP Refresher is based on more than 15 years of Clinical Operations experience and (unlike other courses) provides educational videos, many interactive exercises and learning diaries.
Consequently, you will enjoy this course.

Do I get a certificate?

Yes, you’ll receive a Training Certificate as file download immediately after you assed the last exam.

How long do I have access to the course?

You geet access to the course for 3 months.
So, once purchased, you'll have plenty of time to access and implement all the concepts and materials.

I’m skeptical about the course. Why should I still consider it?

That’s completely understandable. Many Clinical Trial Professionals feel the same way, especially when they’ve already attended generic GCP trainings or read countless regulatory documents.

But here’s the difference:
This course is built on real-world experience, not abstract theory. It combines regulatory compliance from the ICH E6(R3) and ATMP guidelines, personal experience from over 15 years in ATMP clinical trial management, and practical exercises based on real-life scenarios.

If you’re still unsure, ask yourself: “What’s the alternative if I continue without this training?”

If you’re ready to avoid Uncertainty and gain Clarity on ATMP-specific GCP expectations, this course is your shortcut to Confidence and Compliance.

Would it help if I could guarantee that you’ll walk away with actionable insights?
→ Then let’s get started. You’re covered by our satisfaction guarantee.

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