Posters - NCDEU: An Annual Meeting Sponsored by ASCP
Posters - NCDEU: An Annual Meeting Sponsored by ASCP
Posters - NCDEU: An Annual Meeting Sponsored by ASCP
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Featured Speakers<br />
Regulatory Wrap-Up<br />
Friday, June 1st from 10:15 am – 11:45 am<br />
Regulatory Wrap-Up<br />
Thomas Laughren, M.D., Food and Drug Administration<br />
See previous bio<br />
Karl Broich, M.D., Federal Institute for Drugs and Medical Devices<br />
(BfArM, Germany)<br />
See previous bio<br />
Mitchell Mathis, M.D.<br />
Food and Drug Administration<br />
Dr. Mitchell Mathis is the Deputy Director of Division of<br />
Psychiatry Products, Center for Drug Evaluation and Research at<br />
the FDA. He is a graduate of the Uniformed Services University<br />
of the Health Sciences School of Medicine in Bethesda,<br />
Maryland. He trained in family practice at Malcolm Grow<br />
USAF Medical Center in Maryland and in psychiatry at Walter<br />
Reed Army Medical Center in Washington, D.C. He has been<br />
practicing outpatient and emergency room psychiatry in D.C.<br />
and Maryland since 2001. He is board certified <strong>by</strong> the American Board of Psychiatry<br />
and Neurology.<br />
Manuel Haas, PharmD, MSc<br />
European Medical Agency<br />
Manuel Haas is Head of the Central Nervous System and<br />
Ophthalmology section in the European Medicines Agency’s<br />
Safety and Efficacy Sector (Human Medicines Development<br />
and Evaluation Unit). The “CNS” Section is responsible for<br />
the management of pre- and post-authorisation activities<br />
of centralised applications/marketing authorisations, and<br />
particularly the Safety and Efficacy part, related to medicinal<br />
products in the neurology, psychiatry and ophthalmology<br />
therapeutic areas. He is a pharmacist <strong>by</strong> training, and holds a post-graduate diploma<br />
in hospital pharmacy as well as a Masters in Drug Development and Registration.<br />
He worked for several years in hospitals in France and the UK before joining the<br />
pharmaceutical industry in regulatory affairs in 2003. Following this role he started with<br />
the European Medicines Agency in 2004 as Scientific Administrator. He has been in his<br />
current role since September 2009.<br />
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