FDA > CDRH >
Standards Program > Standards Management Staff
Standards Program - Standards Management Staff
Office of the Director
The mission of the Standards Management Staff (SMS) is to:
- manage the participation of CDRH staff in standards development,
- increases the recognition of voluntary consensus standards for medical devices and radiation-emitting electronic products. The Standards Management Program was created as a result of the Food and Drug Administration Modernization Act (FDAMA) of 1997. FDA has adopted Good Guidance Practices (GGP's) which set forth the Agency's policies and procedures for developing, issuing, and using guidance documents.
- manages the participation of other FDA components in medical device standards committees. Maintains a standards database that provides access to established standards to all CDRH staff.
Organization:
Director, SMS |
Carol L. Herman |
240-276-8715 |
Acting Deputy Director |
Susan Meadows |
240-276-8719 |
Public Health Advisor |
Terri D. Bailum |
240-276-8714 |
Public Health Advisor |
Maureen Gallagher |
240-276-8711 |
Standards Coordinator |
Jean M. Olson |
240-276-8717 |
Standards Coordinator |
Norma J. Ryskewich |
240-276-8718 |
Standards Coordinator |
Victoria R. Wagman |
240-276-8720 |
Standards Coordinator |
Laurence K. Hill |
240-276-8716 |
Internet Resources
Updated August 6,
2008
CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page
Center for Devices and Radiological Health / CDRH