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GMP for ATMPs
Delivered at your site

GMP for ATMPs

Updated Tuesday, 10 March 2026 at 10:50

The training is intended for professionals who work with ATMPs and are involved in production, quality control, or quality assurance within pharmaceutical, biotech, or hospital pharmacies.

One trainer, one team, your site

Run for your team at your location. We adapt the material to your products, SOPs and recent inspection findings — taught by the same trainers who run our public PCS Academy courses.

Request a custom training quotation

What's included

  • Programme adapted to your products and SOPs
  • Trainer travels to your site — no staff time lost
  • Dates that fit your production schedule
  • Individual certificate for every participant
  • Same trainers who teach our public PCS Academy courses

Difficulty

Intermediate level

Topics

GMP

Categories

Good Manufacturing Practice (GMP) | GMP Training

What you will learn

You will understand the key GMP principles for ATMPs

You will know the differences between traditional GMP and GMP for cell, tissue, and gene therapy

You will recognize critical risks such as contamination, aseptic working, and traceability

You will know how documentation, deviation management, and change control are applied within ATMP processes

You will be better prepared for audits and inspections

Description

Advanced Therapy Medicinal Products (ATMPs), such as cell and gene therapy, present unique challenges in terms of quality, production, and traceability. In this one-day training course, you will learn how GMP principles are applied within an ATMP environment and what specific risks and points of attention play a role in this. The training combines regulations with practical examples, enabling you to better translate GMP requirements to your own organization and processes.

This training might be subject to change.

Target Audience

The training is intended for professionals who work with ATMPs and are involved in production, quality control, or quality assurance within pharmaceutical, biotech, or hospital pharmacies.

Contents

The training covers the following topics, among others:

  • introduction to ATMPs and GMP
  • differences between traditional GMP and ATMP production
  • facilities, cleanrooms, and aseptic working
  • documentation, batch records, and traceability
  • deviation management, change control, and CAPA
  • roles of QA, QC, and QP within ATMP processes
  • practical examples and cases from the ATMP environment

Programme

Results

After this training, you will have:

  • greater insight into GMP requirements for ATMPs
  • better control over quality and compliance risks
  • a better understanding of how regulations are translated into practice in the workplace
  • greater confidence in preparing for inspections and audits
  • concrete tools for better embedding GMP within ATMP processes

Request a custom training quotation

Tell us a bit about your team — head count, the topics you need covered, your preferred dates and your site location. We will come back with a tailored proposal and price, usually within one working day.