Handle ethical requirements, IRB approval, trial registration, and pre-analysis plans for RCTs. Use when user mentions: research ethics, IRB, informed consent, trial registration, pre-analysis plan, PAP, data security, vulnerable populations, research transparency.
El comando exacto puede variar según el repositorio. Consulta el README en GitHub.
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<skill_content>
<overview>
Ethical research with human subjects requires IRB approval, informed consent, data security, and transparency through trial registration and pre-analysis plans. The Belmont Report establishes three core principles: respect for persons (autonomy, consent), beneficence (maximize benefits, minimize harms), and justice (fair distribution of burdens and benefits). Violations risk participant harm, legal liability, and inability to publish.
Ethics and transparency are prer
[Description truncada. Veja o README completo no GitHub.]
