> Import Safety Summit > HDMA Commends Introduction of HR 6353 > HDMA Commends House Committee Chairmen > HDMA FDAAA Comments > HDMA Testifies Supporting HR5839
print page
9:00 – 9:05 AM
Welcome
Jeffrey Shuren; Assistant Commissioner for Policy, FDA
9:05 – 9:15 AM
Opening Remarks
Janet Woodcock; Deputy Commissioner, Chief Medical Officer, FDA
9:15 – 9:20AM
Meeting Format
Jeffrey Shuren
Presentations by Registered Speakers
9:20 – 9:45 AM
Mr. D. Bruce Cohen; Technical Director, Unit Operations; GlaxoSmithKline (representing PhRMA)
9:45 – 10:10 AM
Mr. Peter Mayberry; Executive Director;Pharmaceutical Printed Literature Association
10:10 – 10:30 AM
Dr. Thomas F. Willer; Director, Global Regulatory Affairs, Hospira
10:30 – 10:50 AM
Mrs. Vera Sharav; President, Alliance for Human Research Protection
10:50 – 11:05 AM
Break
11:05 – 11:30 AM
Mr. John Coster; Vice President, Policy and Programs, NACDS
11:30 – 11:40 AM
Mr. Douglas J. Scheckelhoff; Director, Pharmacy Practice Managers , American Society of Health-System Pharmacists
11:40 AM – 12:00 PM
Dr. Danielle Daignault; Managing Editor, Alchemy DSMs, Gold Standard Inc., An Elsevier Company
12:00 – 1:20 PM
Lunch (on own)
1:20 – 1:45 PM
Dr. Mukesh Mehta; Vice President, Thomson Healthcare
1:45 – 2:10 PM
Ms. Karen Kistler; Genentech, Inc.
2:10 – 2:30 PM
Ms. Anita Ducca; Sr. Director, Regulatory Affairs & Healthcare Policy, Healthcare Distribution Management Association
2:30 – 3:25 PM
Open Public Session Break
3:25 – 3:30 PM
Closing Remarks
3:30 PM
Meeting Adjourned