| Description |
1 online resource (iii, 106 pages) : color illustrations. |
| Series |
S. hrg. ; 117-395
|
|
United States. Congress. Senate.
S. hrg. ; 117-395.
|
| Note |
Access ID (govinfo): CHRG-117shrg48906. |
|
Associated bill citation(s): S. 4071. |
|
In scope of the U.S. Government Publishing Office Cataloging and Indexing Program (C&I) and Federal Depository Library Program (FDLP). |
|
GPO Cataloging Record Distribution Program (CRDP). |
| Bibliography |
Includes bibliographical references. |
| Performer |
Hearing witnesses: Cavazzoni, Patrizia, M.D., Director, Center for Drug Evaluation and Research, United States Food and Drug Administration, Silver Spring, MD; Marks, Peter, M.D., Ph.D., Director, Center for Biologics Evaluation and Research, United States Food and Drug Administration, Silver Spring, MD; Shuren, Jeffrey, M.D., J.D., Director, Center for Devices and Radiological Health, United States Food and Drug Administration, Silver Spring, MD. |
| Event |
Date of hearing: 2022-04-26. |
| Subject |
User charges -- United States.
|
|
Drug approval -- United States.
|
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Medical supplies -- Certification -- United States.
|
| Genre/Form |
Legislative hearings.
|
| Other Form: |
Print version: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions. FDA user fee agreements: advancing medical product regulation and innovation for the benefit of patients, FDA center directors (OCoLC)1409349004 |
| Standard No. |
48-906 (GPO jacket number) |
| Gpo Item No. |
1043-C (online) |
| Sudoc No. |
Y 4.L 11/4:S.HRG.117-395 |
|
