Main Menu     Training     Advanced Training    

GMP Virtual Hands-On Workshop

The highly acclaimed Hands-on Good Manufacturing Practices (GMP) Workshop is now offered in a new interactive e-learning format. This course is designed for cell biologists, research scientists, process engineers, quality assurance specialists, technologists and trainees (and other end users) who are working, or plan to work in areas associated with the manufacturing of cell and gene therapies, or want to expand their knowledge on advancing cell and gene therapy projects towards the clinic.

--> Buy now

At the end of this course, the participants will be able to:

  • Identify the essentials of GMP requirements and the relevant Canadian and international regulations;
  • Identify cleanroom facility and gowning requirements and define aseptic workflow;
  • Identify the components of a recognized GMP training program;
  • Recall the main components of a Quality Management Systems (QMS), including SOP writing and quality manual development, batch records, environmental monitoring and GMP training program;
  • Describe how to plan a validation strategy through Quality by Design and Risk Management;
  • Explain basic manufacturing techniques for cell-based therapies;
  • Identify the quality control steps and parameters required for product release.

 More than 12 hours of interactive training
 Learn at your own pace and in the comfort of your own home
 Test your knowledge through assessments and quizzes
 Pass the exam and obtain your certificate of completion
 Add to your HQP training file for regulatory compliance
 Interact with our experts and network with other trainees 


Wondering what Good Manufacturing Practices (GMP) is all about?


Take our Essentials of CGT GMP manufacturing in under 60 minutes course and you’ll have a basic understanding of what manufacturing under GMP means! 

At the end of this course, learners will be able to:

  • Explain how production under GMP differs from routine laboratory work, including process development;
  • Identify the main components of Quality Management Systems (QMS) required to manufacture biotherapeutics under GMP;
  • Describe the critical path and steps to translate process development into GMP production: minimizing risk.
  • This course is also available in French.
    60 minutes of training
  Learn at your own pace and in the comfort of your own home
  Test your knowledge through assessments and quizzes 
   Pass the exam and obtain your certificate of completion



Upcoming training offers

Looking to work in CGT manufacturing or in need of field-specific retraining? Increasing your HQP workforce for your manufacturing facility? Many advanced training offers for various job roles (executives, QA, QC, operators) are in preparation.

Founded in 2014, CellCAN has trained over 250 highly qualified personnel (HQP) and offers unique training on GMP manufacturing throughout Canada. We educate users on why, when and how to engage GMP manufacturing centres in the process of creating a clinical product.

Our network of cell manufacturing facilities (CMF) allows us to tap into world-class expertise, provide unique training opportunities, and offer hands-on learning experiences. CellCAN brings together Canada’s leading experts in regenerative medicine and cell and gene therapy (RMCT) and gives our trainees the opportunity to network with them.

To learn more about our training & make sure you don't miss any opportunities, subscribe to our email list and/or contact us via our Helpdesk.  


Connect with a network of Canadian researchers, clinicians, regulatory experts and HQP from coast to coast, through our platforms, workshops and events.