Archive for the 'by Nancy Walton' Category

Bill Jenkins and the legacy of the Tuskegee Syphilis Study

• March 3, 2019 • Leave a Comment

Posted in by Nancy Walton, consent, trial design, vulnerable populations


A call for “new rules” for Internet-based research

• September 16, 2014 • Leave a Comment

Posted in by Nancy Walton, children, consent, internet-based research


Research ethics scandals in Canada, you ask? Sadly, yes.

• July 23, 2013 • 1 Comment

Posted in by Nancy Walton, children, consent, ethics committees, justice, poverty, recruitment, regulations, review, scientists, vulnerable populations


Research Fraud Case Raises Concerns Over Ethics of Psychology Research

• November 15, 2011 • 1 Comment

Posted in by Nancy Walton, clinical trials, database, ethics committees, international, regulations, scientists, Uncategorized


What Scorpion Bites Can Teach Us About Placebo Trials

• August 14, 2011 • Leave a Comment

Posted in by Nancy Walton, children, clinical trials, consent, pharmaceuticals, recruitment


Prenatal Surgery, Hope for Spina Bifida and Ethical Reflection

• February 15, 2011 • 1 Comment

Posted in by Nancy Walton, children, clinical trials, consent, ethics committees, neurological, recruitment


German Anesthetist Faces Massive Retraction of Published Research Articles

• February 14, 2011 • Leave a Comment

Posted in by Nancy Walton, clinical trials, ethics committees, international, regulations, review, scientists


Parents Complain Over “Opt-Out” Consent In Kindergarten Study

• February 6, 2011 • 4 Comments

Posted in by Nancy Walton, children, consent, data sharing, ethics committees, review


Tragedy and the Clinical Trial: Part 2

• November 21, 2010 • Leave a Comment

Posted in by Nancy Walton, clinical trials, pharmaceuticals, recruitment


A Tale of Two Cousins: Tragedy and the Clinical Trial

• October 1, 2010 • 7 Comments

Posted in by Nancy Walton, clinical trials, ethics committees, pharmaceuticals, regulations, scientists, Uncategorized


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