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E-BOOK
Title Compact REGS parts 50, 54, 56, and 312 : cfr 21 parts 50, 56, and 312 good clinical practices (10 pack) / edited by Interpharm.
Imprint Boca Raton, FL : Taylor and Francis, an imprint of CRC Press, 2013.

Copies/Volumes

LOCATION CALL # STATUS
 Internet  Electronic Book    AVAILABLE
Edition Second edition.
Description 1 online resource (24 pages)
Bibliog. Includes bibliographical references and index.
Note Available only to authorized UTEP users.
Subject Clinical trials -- Law and legislation -- United States.
Clinical trials -- Law and legislation.
Drugs -- Testing -- Law and legislation -- United States.
Drugs -- Testing -- Law and legislation.
Human experimentation in medicine -- Law and legislation -- United States.
Human experimentation in medicine -- Law and legislation.
United States.
Contents Chapter PART 50--PROTECTION OF HUMANSUBJECTS -- chapter PART 54--FINANCIAL DISCLOSURE BYCLINICAL INVESTIGATORS -- chapter PART 56--INSTITUTIONAL REVIEWBOARDS -- chapter PART 312--INVESTIGATIONAL NEW DRUGAPPLICATION.
Summary This publication contains a verbatim reproduction of 21 CFR Part 50 Protection of Human Subjects, 21 CFR Part 54 Financial Disclosure by Clinical Investigators, 21 CFR Part 56 Institutional Review Boards & 21 CFR Part 312 Investigational New Drug Application.
Other Author Interpharm, editor.