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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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