CDRH - Office of in Vitro Diagnostic Device Evaluation and Safety - Organization - Text version
The following header reflects the organizational hierarchy.
FOOD AND DRUG ADMINISTRATION
OFFICE OF MEDICAL PRODUCTS AND TOBACCO
CENTER FOR DEVICES AND RADIOLOGICAL HEALTH
OFFICE OF IN VITRO DIAGNOSTICS AND RADIOLOGICAL HEALTH
The following is the communication box containing information to assist anyone who may want to communicate with the depicted organization via telephone, facsimile or mail.
301 847- 8513
WO Bldg 66 Rm 5680
10903 New Hampshire Ave.
Silver Spring, MD 20993
The following is the Food and Drug Administration, Center for Devices and Radiological Health, Office of In Vitro Diagnostics and Radiological Health organization structure depicting all the organizational structures reporting to the Office Director. These organizational structures are organized in sequential order by their assigned Standard Administrative code (Alphanumeric sequence of characters beginning with the letter D).
Each organizational component will be depicted in the following standard format:
Title of organization.
Position title of the manager.
Military rank if any, first name, middle initial if any, last name, post graduate degrees if any, and if the individual is designated as acting.
Standard Administrative code.
Alberto Gutierrez, Ph.D.
Reports directly to the Office of In Vitro Diagnostics and Radiological Health Director
Deputy Director for New Product Evaluation
Donald J. St. Pierre
Deputy Director for Patient Safety and Product Quality
James L. Wood
Deputy Director for Radiological Health
Mary S. Pastel, Sc.D.
Chief Medical Officer for In Vitro Diagnostics
Robert Becker, M.D.
Director for Personalized Medicine
Elizabeth A. Mansfield, Ph.D.
Approved by the FDA Reorganization Coordinator and Principal Delegation Control Officer