This is the third post in our five-part series explaining the new global guidelines (ICH E6(R3)) through real patient experience, not complicated policy terms. Before someone joins a clinical study, they’re asked to sign an informed consent form. In theory, this form is supposed to help people understand: 🌀 What the study is about and what will be asked of them. 🌀 What the potential risks are. 🌀 That they have the absolute right to say "no." The Reality Gap That’s the
1 day ago2 min read
"If no one else was telling their story, then maybe I needed to tell mine. And maybe, just maybe, that would give others permission to share theirs too."
