3. Will I learn about ethics, consent, and responsible reporting?

Q: 3. Will I learn about ethics, consent, and responsible reporting?

Yes—it includes a full module dedicated to ethics , covering concepts like equipoise, IRBs, informed consent, HIPAA, and landmark ethics documents. You'll also learn the CONSORT guidelines —the gold standard for transparent and rigorous clinical trial reporting. This gives you tools to critically evaluate published trials, not just design them. Additionally, you'll develop a well-rounded awareness of how ethics and reporting influence trial validity and public trust.

Yes—it includes a full module dedicated to ethics, covering concepts like equipoise, IRBs, informed consent, HIPAA, and landmark ethics documents.
You’ll also learn the CONSORT guidelines—the gold standard for transparent and rigorous clinical trial reporting.
This gives you tools to critically evaluate published trials, not just design them.
Additionally, you’ll develop a well-rounded awareness of how ethics and reporting influence trial validity and public trust.