Skip to primary content

Research Ethics.ca

Research Ethics.ca

Main menu

  • Home
  • About
    • About Nancy Walton
  • Books
  • Canada
  • Children and Youths
  • Corporate Research
  • International
  • Social Sciences & Humanities
  • What Is Research Ethics?

International

Institutions / Organizations

  • The NIH Office of Human Subjects Research(U.S.)
  • European Network of Research Ethics Committees
  • Public Responsibility in Medicine & Research
  • Office of Research Integrity, Dept. of Health and Human Services (U.S.)
  • Alliance for Human Research Protection
  • World Health Organization (WHO): Ethics & Health
  • UNESCO: Ethics of Science & Technology

Key Documents

    • Declaration of Helsinki
    • The Nuremberg Code
    • The “Common Rule” (U.S.)
    • Belmont Report (U.S.)

 

  • International Ethical Guidelines for Biomedical Research Involving Human Subjects (CIOMS)
  • Basic HHS Policy for Protection of Human Research Subjects (U.S.)
  • Operational guidelines for ethics committees that review biomedical research (WHO)

 

Articles

  • “Placebos: Deceptive benefits” (Jeffrey P. Kahn,CNN: Ethics Matters, November 27, 2000)
  • “A University Wide Model for the Ethical Review of Human Subjects Research” (Bryn Williams-Jones & Soren Holm, Research Ethics Review,2005, Vol 1, No 2, 39–44)
  • “Higher Standards for Privately Funded Health Research” (Chris MacDonald, Canadian Bioethics Society Newsletter, Vol. 9, No. 1, February 2004)
  • “Sugar Pills vs Medicine: The Ethics Behind Placebo-Controlled Trials” (Chris MacDonald,Parkhurst Exchange, January 2002)

 

Share this:

  • Twitter
  • Facebook

Like this:

Like Loading...
Blog at WordPress.com.
  • Follow Following
    • Research Ethics.ca
    • Already have a WordPress.com account? Log in now.
    • Research Ethics.ca
    • Customize
    • Follow Following
    • Sign up
    • Log in
    • Copy shortlink
    • Report this content
    • View post in Reader
    • Manage subscriptions
    • Collapse this bar
%d bloggers like this: