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.

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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

CellCAN-flyerTraining.pdf