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alterlab-research-ethics

Creates research ethics plans covering consent, data management, and compliance for IRB submissions and GDPR/HIPAA regulations.

58|9|Updated Mar 16, 2026
Search Tags:#ethics#GDPR#HIPAA#data-management#IRB#consent#research-integrity
One-click install
npx skills add https://github.com/AlterLab-IEU/AlterLab-Academic-Skills --skill alterlab-research-ethics
Or copy as Structured Prompt for Agent▼
Please help me install this Agent Skill.
Skill: alterlab-research-ethics
Source: https://github.com/AlterLab-IEU/AlterLab-Academic-Skills/tree/main/skills/research-tools/alterlab-research-ethics
Command: npx skills add https://github.com/AlterLab-IEU/AlterLab-Academic-Skills --skill alterlab-research-ethics

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) components.

What problem does it solve?

This skill provides a structured, practical framework to navigate research ethics, regulatory requirements, and integrity throughout the research lifecycle, helping researchers design compliant studies and communicate ethics considerations clearly.

Core Features & Use Cases

  • Foundational ethical principles: Belmont Report, Declaration of Helsinki, and Singapore Statement guidance for responsible research.
  • Ethics board applications and informed consent: templates and checklists to prepare IRB submissions and consent materials.
  • Data governance and regulatory compliance: guidance on GDPR, HIPAA, data minimization, and data management planning.
  • Vulnerable populations and research integrity: frameworks for protecting participants, addressing conflicts of interest, and DURC considerations.

Quick Start

Provide your study details to generate an ethics plan and consent materials.

Frequently Asked Questions about alterlab-research-ethics

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

FAQPage Schema
How do I draft an IRB submission and informed consent materials for research?▼

Drafting an IRB submission and informed consent involves structuring your study details to generate an ethics plan and consent materials. This framework provides templates and checklists aligned with Belmont and Helsinki principles to prepare regulatory documentation.

How do I ensure GDPR and HIPAA compliance in my research data management plan?▼

Ensuring GDPR and HIPAA compliance requires integrating data minimization and governance strategies into your data management plan. This framework guides regulatory adherence for data protection throughout the research lifecycle.

Does this research ethics framework support studies involving vulnerable populations?▼

Yes, this research ethics framework supports vulnerable populations by applying targeted protection protocols. It structures guidelines for research integrity and conflict of interest management within studies involving at-risk participants.

What's the best way to structure a research ethics plan for DURC considerations?▼

The best way to structure a research ethics plan for DURC is to apply actionable frameworks mapping dual use research of concern guidelines. This ensures research integrity scenarios are addressed alongside standard compliance requirements.

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