Bill Jenkins and the legacy of the Tuskegee Syphilis Study

It’s been a while – a LONG while – but here goes a renewed effort to try to keep people engaged in all things research ethics. It’s a busy time of life for us, with a ton of demands, but I’m feeling a strong pull towards trying to rekindle the Research Ethics Blog. Let’s start […]

Source: blog.bioethics.net - March 3, 2019 Category: Medical Ethics Authors: Nancy Walton Tags: Health Care by Nancy Walton consent syndicated trial design vulnerable populations Source Type: blogs