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FDA user fee reauthorization : ensuring safe and effective medical devices : hybrid hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Seventeenth Congress, second session, March 30, 2022.
- Format:
- Book
- Government document
- Author/Creator:
- United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health, author.
- Language:
- English
- Subjects (All):
- United States. Food and Drug Administration.
- United States.
- User charges--United States.
- User charges.
- Drug approval--United States.
- Drug approval.
- Medical supplies--Certification--United States.
- Medical supplies.
- Genre:
- Legislative hearings.
- Physical Description:
- 1 online resource (v, 123 pages) : color illistrations
- Other Title:
- Ensuring safe and effective medical devices
- Food and Drug Administration user fee reauthorization
- Place of Publication:
- Washington : U.S. Government Publishing Office, 2026.
- Participant:
- Hearing witnesses: Jeff Shuren, M.D., Director, Center for Devices and Radiological Health, Food and Drug Administration; Richard J. Kovacs, M.D., Q.E. and Sally Russell Professor of Medicine, Indiana University School of Medicine, Chief Medical Officer, American College of Cardiology; Mark Leahey, President and CEO, Medical Device Manufacturers Association; Janet Trunzo, Senior Executive Vice President, Technology And Regulatory Affairs, Advanced Medical Technology Association; Diane Wurzburger, Executive of Regulatory Affairs, GE Healthcare.
- Notes:
- This is a publication issued by the United States federal government or produced with federal funds.
- Associated bill citation(s): H.R. 7084; H.R. 7192.
- "Serial no. 117-77."
- Includes bibliographical references.
- Date of hearing: 2022-03-30.
- Description based on online resource, PDF version; title from title page (GovInfo, viewed Mar. 12, 2026).
- In scope of the U.S. Government Publishing Office Cataloging and Indexing Program (C&I) and Federal Depository Library Program (FDLP).
- Other Format:
- Print version: United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health. FDA user fee reauthorization
- OCLC:
- 1579072155
- Publisher Number:
- 60-330 (GPO jacket number)
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