ethics-committee

Analyze research protocols for ethical compliance and regulatory requirements.

8|2|Updated May 10, 2026
One-click install
npx skills add https://github.com/Marazii/research-co-pilot --skill ethics-committee
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: ethics-committee
Source: https://github.com/Marazii/research-co-pilot/tree/main/skills/ethics-committee
Command: npx skills add https://github.com/Marazii/research-co-pilot --skill ethics-committee

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) components.

What problem does it solve?

This Skill helps researchers pre-assess their study protocols for ethical considerations, reducing the risk of rejection or delays during formal review processes.

Core Features & Use Cases

  • Protocol Review Simulation: Acts as a research ethics committee to identify ethical issues in the protocol, consent forms, and recruitment materials.
  • Guidance on Compliance: Provides tailored feedback according to jurisdiction-specific frameworks like US, EU, UK, or Canada.
  • Use Case: A researcher preparing an IRB submission can input their protocol draft and receive a comprehensive ethics review to address potential concerns preemptively.

Quick Start

Upload your protocol draft or IRB application and ask for an ethics review to get detailed feedback on compliance and ethical considerations.

Frequently Asked Questions about ethics-committee

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I pre-assess a research protocol for IRB compliance before formal submission?

Pre-assessing a research protocol for IRB compliance involves analyzing study designs, consent forms, and recruitment materials against regulatory requirements to identify ethical issues before formal submission.

Can I get ethics review feedback tailored to specific regulatory frameworks like the US or EU?

Ethics review feedback can be tailored to jurisdiction-specific frameworks including US, EU, UK, and Canada, ensuring research protocols meet regional regulatory compliance and participant protection standards.

What components of a research study does an ethics review typically analyze?

An ethics review analyzes research protocols, consent forms, and recruitment materials to identify ethical issues, verify participant protection, and ensure regulatory compliance across multiple jurisdictions.

Does a simulated ethics review replace the need for a formal IRB submission?

A simulated ethics review does not replace a formal IRB submission. It serves as a pre-assessment to strengthen study design and documentation, reducing the risk of rejection or delays during the formal review.

How do I prepare an IRB application draft to identify potential ethical issues preemptively?

Preparing an IRB application draft for ethical review involves compiling study design, consent forms, and recruitment materials, then inputting the draft to receive detailed feedback on participant protection and regulatory compliance.