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Mission Statement: The mission of the European Legal and Regulatory Affairs Committee is to serve those working in the field of cellular and gene therapy by being a source of information regarding compliance with EU directives, local and professional regulations and by being a voice in the moderation of external regulation.
Duties: The committee will:
- keep members up to date on potential and actual changes in regulatory affairs and respond to the authorities in open consultations on behalf of the membership;
- recommend revision of standards to JACIE;
- provide information to members to assist with compliance with standards;
- organize workshops and communicate current and future needs for regulatory affairs issues to other committees or to the board of directors.
Chair:
Ineke Slaper-Cortenbach, PhD
Utrecht, The Netherlands
i.slaper@azu.nl
Committee Members:
Christian Chabannon, MD, PhD
Marseille, France
Doris Herrmann, PhD
Heidelberg, Germany
Martino Introna, MD
Bergamo, Italy
Pedro Marin, MD
Barcelona, Spain
Mike Scott, PhD, MSc
Cambridge, UK
Panteli Theocharous, BSc, MSc, PhD
Bucks, UK
Koen Theunissen, MD
Leuven, Belgium
Recent Activities:
Input into annual meeting content.
Abstract review and scoring.
Regulatory Affairs Europe Resources
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