Archive for the 'consent' Category
Bill Jenkins and the legacy of the Tuskegee Syphilis Study
• March 3, 2019 • Leave a CommentPosted in by Nancy Walton, consent, trial design, vulnerable populations
A call for “new rules” for Internet-based research
• September 16, 2014 • Leave a CommentPosted in by Nancy Walton, children, consent, internet-based research
Research ethics scandals in Canada, you ask? Sadly, yes.
• July 23, 2013 • 1 CommentPosted in by Nancy Walton, children, consent, ethics committees, justice, poverty, recruitment, regulations, review, scientists, vulnerable populations
Clinical Trials in Russia
• November 12, 2012 • Leave a CommentPosted in by Chris MacDonald, clinical trials, consent, international, poverty, recruitment
What Scorpion Bites Can Teach Us About Placebo Trials
• August 14, 2011 • Leave a CommentPosted in by Nancy Walton, children, clinical trials, consent, pharmaceuticals, recruitment
Prenatal Surgery, Hope for Spina Bifida and Ethical Reflection
• February 15, 2011 • 1 CommentPosted in by Nancy Walton, children, clinical trials, consent, ethics committees, neurological, recruitment
Parents Complain Over “Opt-Out” Consent In Kindergarten Study
• February 6, 2011 • 4 CommentsPosted in by Nancy Walton, children, consent, data sharing, ethics committees, review
Could Research be Done on Trapped Miners?
• August 29, 2010 • 3 CommentsPosted in by Chris MacDonald, consent, recruitment, vulnerable populations
Research Ethics Blog 