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09:00 - 17:00 23 January 2013

REGULATORY AND TRANSLATIONAL ASPECTS OF MANAGING CELL AND GENE THERAPY CLINICAL TRIALS

Location

UCL Institute of Child Health (link Map)
30 Guilford Street | London | WC1N 1EH |

Open to: Academic
Ticketing: Pre-booking essential

This one day CPD course is suitable for those interested in setting up and managing clinical trials of advanced therapeutic medicinal products, such as cell and gene therapy. Delivered as part of an MSc in Cell and Gene Therapy, this one day meeting is suitable for researchers and managers from academia and industry who would like to understand the regulatory aspects involved in running a clinical trial in this area. Subjects covered include:

 * Regulatory requirements
* Manufacture of products to Good Manufacturing Practice (GMP) standards
* Practical aspects of initiating and managing gene and cell therapy clinical trials
* The Human Tissue Act
* Ethics
* Examples of trials and translation from Industry

Continuing Professional Development points (CPD) will be available for attendance at this meeting.


Contact

Amanda Kosinski
please email | a.kosinski@ucl.ac.uk


Links

More information and registration for the meeting