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Designing a Cell Therapy Production Process

 
  June 28, 2017  
     
 
CfPA-The Center for Professional Advancement, Online Live
August 30, 2017 at 11:00 a.m.–12:30 p.m. (ET)


Who Should Attend?
This online training will benefit professionals in the following industries:Biotechnology – Scientists, Managers, Technicians, Engineers, Auditors

In departments such as: Research and Development, Manufacturing, Regulatory, Operations, QA/QC, Clinical

Course Description
This 90-minute accredited training will provide an overview of the process required for manufacturing cellular therapies. It will highlight the considerations to be made when designing production. The availability of products that meet patient needs when required can be paramount to the success of a trial. This course will help you to select the correct equipment, consumables and reagents to meet regulatory requirements, reduce costs and mitigate risks. Furthermore, to highlight the importance of planning for large scale manufacturing early to reduce the need to make manufacturing process changes during clinical trials.
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
Dr. Louisa Mathias, Production Manager, Cell Medica, London, UK

Dr. Louisa Mathias has experience manufacturing a variety of cellular therapies including ATMPs and blood products under MHRA, HTA, TGA and FACT requirements and standards. In her roles as head of production, she has been responsible for overseeing the manufacturing process from collection through to release. Having completed a PhD in Immunology, she has a sound understanding of cell biology and the relevant tests required for these products. Dr. Mathias has experience tutoring and mentoring students and staff in the technical aspects of cell processing and quality control assays. 

 


 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
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