FDA user fees and the regulation of drugs, biologics, and devices : comparative analysis of S. 3187 and H.R. 5651 / Susan Thaul [and six others].

Format:

Government document

Website/Database

Author/Creator:

Thaul, Susan, author.

Contributor:

Library of Congress. Congressional Research Service, issuing body.

Series:

CRS report ; R42564.

Report / Congressional Research Service ; R42564

Language:

English

Subjects (All):

United States. Food and Drug Administration--Rules and practice.

United States.

United States. Food and Drug Administration Safety and Innovation Act.

United States. Food and Drug Administration.

Food and Drug Administration Safety and Innovation Act (United States).

Medical instruments and apparatus industry--Law and legislation--United States.

Medical instruments and apparatus industry.

Drugs--Prices--Law and legislation--United States.

Drugs.

Medical instruments and apparatus--United States--Costs.

Medical instruments and apparatus.

User charges--Government policy--United States.

User charges.

Drugs--Prices--Law and legislation.

Medical instruments and apparatus--Costs.

Medical instruments and apparatus industry--Law and legislation.

User charges--Government policy.

Genre:

Bibliographies.

bibliographies.

Rules.

Physical Description:

1 online resource.

Updated irregularly

Edition:

[Library of Congress public edition].

Other Title:

Food and Drug Administration user fees and the regulation of drugs, biologics, and devices

Comparative analysis of S. 3187 and H.R. 5651

Place of Publication:

[Washington, D.C.] : Congressional Research Service, 2018-

Notes:

The CRS report home page provides access to all versions published since 2018 in accordance with P.L. 115-141; earliest version dated 2012.

Report includes bibliographical references.

Description based on contents viewed on Jan. 21, 2020; title from CRS report home page.

OCLC:

1137387541