This workshop aims to examine potential biomarkers, discuss the challenges and solutions related to biomarker development methodologies, and establish strategies for data standardization, sharing and analysis of big data sets for Traumatic Brain Injury (TBI). By convening the relevant stakeholders, the goal is to obtain input on the scientific, clinical, patient and regulatory considerations associated with TBI biomarker development to improve diagnosis and clinical utility for TBI.
- Date, Time and Location
- Federal Register Notice
- Webcast
- Registration
- Contact Us
Date, Time and Location
This meeting will be held March 3, 2016, beginning at 8:00 am – 5:00 pm at the following location:
FDA White Oak Campus
10903 New Hampshire Avenue
Bldg. 31, Room 1503 (the Great Room)
Silver Spring MD, 20993
- FDA Campus Information
Webcast
The meeting will be webcast. The webcast link will be available on this web page after February 25, 2016.
If you have never attended a Connect Pro event before, test your connection at https://collaboration.fda.gov/common/help/en/support/meeting_test.htm. To get a quick overview of the Connect Pro program, visit http://www.adobe.com/go/connectpro_overview.
Registration to Attend the Workshop
If you wish to attend this Workshop, you must register by 4:00 pm on February 25, 2016.
There is no fee to register for the Workshop and registration will be on a first-come, first-served basis. Seating is limited so early registration is recommended.
Contact Us
If you require special accommodations due to a disability, or need additional information regarding registration, please contact Susan Monahan, Office of Communication and Education, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Avenue, Bldg. 32, Silver Spring, MD 20993, 301-796-5661, [email protected].
For questions regarding workshop content please contact:
Allison Kumar, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave, Bldg. 66 rm. 5408, Silver Spring, MD 20993, 301-796-6369, email: [email protected]; or
Lakshmi Kannan, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, rm. 5402, Silver Spring, MD 20993, 240-402-7735, email: [email protected]