Public Meeting - Regulatory Science Considerations for Medical Countermeasure Radiation Biodosimetry Devices, September 27-28, 2012

The Food and Drug Administration (FDA) is announcing a public meeting entitled "Regulatory Science Considerations for Medical Countermeasure Radiation Biodosimetry Devices." The purpose of this meeting is to obtain input from academia, Government, industry and other stakeholders on the clinical application and scientific and technological challenges for performance validation of radiation biodosimetry devices.

• Date, Time and Location
• Federal Register Notice
• Webcast
• Agenda
• Registration
• Contact Us

Date, Time and Location

This meeting will be held September 27-28, 2012 from 8:00 a.m. - 5:00 p.m. at the following location:

FDA White Oak Campus
10903 New Hampshire Avenue
Building 31 Conference Center (Great Room, Room 1503)
Silver Spring, MD 20993

• FDA Campus Information

The meeting will be webcasted.

Webcast

The webcast will be available at:

• Webcast for September 27
• Webcast for September 28
• Adobe Connect

Agenda

This is a draft agenda. Speaker names and final topics will be added as details are finalized.

Registration to Attend the Workshop

Online registration is closed as of September 13, 2012.

There is no fee to register for the Workshop and registration will be on a first-come, first-served basis. Early registration is recommended because seating is limited.

If you wish to make an oral presentation during an open comment session at the meeting you must indicate this at the time of registration. FDA requests that presentations focus on the areas defined in the Federal Register Notice. You should also identify which discussion topic you wish to address in your presentation and you must submit a brief statement that describes your experience and/or expertise relevant to your proposed presentation. In order to keep each open session focused on the discussion topic at hand, each oral presentation should address only one discussion topic. FDA will do its best to accommodate requests to speak.

If you require special accommodations due to a disability, or need additional information regarding registration, please contact Joyce Raines, Office of Communications, Education, and Radiation Programs, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Avenue, WO-66 Room 4319, Silver Spring, MD 20993, 301-796-5709, FAX: 301-847-8142, email: joyce.raines@fda.hhs.gov.

Contact Us

For questions regarding workshop content please contact:

Jennifer Dickey
Center for Devices and Radiological Health
Food and Drug Administration
10903 New Hampshire Avenue, WO-66 Room 4254
Silver Spring, MD 20993
301-796-5028
email: Jennifer.dickey@fda.hhs.gov