Information sheet : guidance for institutional review boards and clinical investigators (frequently asked questions).

Information sheet : guidance for institutional review boards and clinical investigators (treatment use of investigational drugs).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (payment to research subjects).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (recruiting study subjects).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (use of investigational products when subjects enter a second institution).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators ("off-label" and investigational use of marketed drugs, biologics, and medical devices).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (continuing review after study approval).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (screening tests prior to study enrollment).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (a guide to informed consent).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (acceptance of foreign clinical studies).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (exception from informed consent for studies conducted in emergency settings; regulatory language and excerpts from preamble).
Published: (1998)

Information sheet guidance for sponsors, clinical investigators, and IRBs : frequently asked questions, statement of investigator (form FDA 1572).
Published: (2008)

Guidance for institutional review boards (IRBs) : frequently asked questions, IRB registration.
Published: (2009)

Guidance for industry : IRB review of stand-alone HIPAA authorizations under FDA regulations.
Published: (2003)

Guidance for clinical investigators, sponsors, and IRBs : adverse event reporting to IRBs : improving human subject protection.
Published: (2009)

Guidance for industry and clinical investigators : the use of clinical holds following clinical investigator misconduct.
Published: (2004)

Institutional review boards in the U.S.-México border : current protocols and practices.
Published: (2010)

Guidance for clinical investigators, institutional review boards, and sponsors : process for handling referrals to FDA under 21 CFR 50.54 : additional safeguards for children in clinical investigations.
Published: (2006)

Guidance for industry : protecting the rights, safety and welfare of study subjects : supervisory responsibilities of investigators.
Published: (2007)

Information sheet guidance for IRBs, clinical investigators, and sponsors : frequently asked questions about medical devices.
Published: (2006)

Human subjects research : undercover tests show the institutional review board system is vulnerable to unethical manipulation : testimony before the Subcommittee on Oversight and Investigations, Committee on Energy and Commerce, House of Representatives /
by: Kutz, Gregory D.
Published: (2009)

Guidance for industry : financial disclosure by clinical investigators.
Published: (2001)

Institutional review boards that oversee experimental human testing for profit : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh Congress, first session, March 26, 2009.
Published: (2012)

Institutional review board member handbook /
by: Amdur, Robert J.
Published: (2007)

Maintaining research integrity : a systematic review of the role of the institutional review board in managing conflict of interest /
by: Shekelle, Paul G.
Published: (2012)

Evaluation of Mortgagee Review Board enforcement actions /
Published: (2009)

Paperwork reduction oversight : hearing before the Subcommittee on Federal Spending, Budget, and Accounting of the Committee on Governmental Affairs, United States Senate, One Hundredth Congress, first session, the Florida demonstration product on research productivity, April 14, 1987, Orlando, FL.
Published: (1988)

Ethical imperialism : institutional review boards and the social sciences, 1965-2009 /
by: Schrag, Zachary M.
Published: (2010)

Ethical imperialism : institutional review boards and the social sciences, 1965-2009 /
by: Schrag, Zachary M.
Published: (2010)

Institutional review board : member handbook /
by: Amdur, Robert J.
Published: (2011)

Health care systems and comparative manpower policies /
by: Roemer, Milton Irwin, 1916-2001
Published: (1981)

Use of commercial institutional review boards in sponsored research trials /

The National Institutes of Health : a review of its reforms, priorities, and progress : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, second session, June 21, 2012.
Published: (2012)

Health care licensing boards.
Published: (1992)

Understanding the IRB.
Published: (2015)

Variations in medical practice : hearing before a subcommittee of the Committee on Appropriations, United States Senate, Ninety-eighth Congress, second session : special hearing.
Published: (1985)

NIH Reform Act of 2006 : progress, challenges, and next steps : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, September 9, 2008.
Published: (2010)