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

Information sheet : guidance for institutional review boards and clinical investigators (non-local IRB review).
Published: (1998)

Information sheet : guidance for institutional review boards and clinical investigators (charging for investigational products).
Published: (1998)

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 (continuing review after study approval).
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 (screening tests prior to study enrollment).
Published: (1998)

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

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

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

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

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

Oversight of NIH and FDA : bioethics and the adequacy of informed consent : hearing before the Subcommittee on Human Resources of the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fifth Congress, first session, May 8, 1997.
Published: (1997)

Guidance for industry : informed consent recommendations for source plasma donors participating in plasmapheresis and immunization programs.
Published: (2007)

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

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

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

Informed consent, judicial review, and the uncertainties of ethnographic research in sensitive National Health Service settings /
by: Hughes, David
Published: (2018)

Informed consent : legal theory and clinical practice /
by: Appelbaum, Paul S.
Published: (1987)

Informed consent : a guide for health care providers /
by: Rosoff, Arnold J.
Published: (1981)

Informed consent : July 1977 through July 1982, 394 citations in English /
by: Kenton, Charlotte
Published: (1982)

Informed consent to human experimentation : the subject's dilemma /
by: Annas, George J.
Published: (1977)

Informed consent in clinical studies post-pandemic : transitioning to e-consenting virtually.
Published: (2021)

How to understand and gain informed consent for internet research /
by: Salmons, Janet, 1952-
Published: (2022)

Informed consent : legal theory and clinical practice.
by: Berg, Jessica W., et al.
Published: (2020)

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

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

A history and theory of informed consent /
by: Faden, Ruth R.
Published: (1986)

Ending the document game : connecting and transforming your healthcare through information technology /
Published: (2005)

The Surfactant, Positive Pressure, and Oxygenation Randomized Trial (SUPPORT) /
by: Buchanan, Lisa R.
Published: (2013)

Assessing for quality informed consent with subjects enrolling in clinical research /
by: Holtz, Laura R.
Published: (2020)

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)

Informed consent in medical therapy and research /
by: Barber, Bernard
Published: (1980)