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medical-standards

Align medical studies with ethics, privacy, terminology, and authorship standards.

Updated Mar 19, 2026
Search Tags:#ethics#gdpr#mesh#hipaa#irb#medical-research#icmje-authorship
One-click install
npx skills add https://github.com/sencersoylu/scholar-flow --skill medical-standards
Or copy as Structured Prompt for Agent▼
Please help me install this Agent Skill.
Skill: medical-standards
Source: https://github.com/sencersoylu/scholar-flow/tree/main/skills/discipline/medical-standards
Command: npx skills add https://github.com/sencersoylu/scholar-flow --skill medical-standards

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

Medical researchers often struggle to ensure studies meet evolving ethical, privacy, terminology, and authorship standards. This skill provides a consolidated reference to ethics frameworks, privacy regulations, standardized terminology, and authorship attribution guidelines to streamline compliance in medical research.

Core Features & Use Cases

  • Ethics and regulatory alignment: Declarations, IRB review, informed consent, data privacy, and vulnerable populations protections.
  • Terminology and authorship: MeSH terminology, ICD coding guidance, and ICMJE/CRediT roles for transparent attribution and indexing.
  • Use Case: When designing a protocol or drafting a manuscript, apply the standards to ensure compliant study design, data handling, and reporting.

Quick Start

Apply the outlined ethics, privacy, terminology, and authorship standards to a new clinical study protocol.

Frequently Asked Questions about medical-standards

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

FAQPage Schema
How do I align my clinical study protocol with the Declaration of Helsinki and HIPAA regulations?▼

To align clinical study protocols with the Declaration of Helsinki and HIPAA regulations, you codify ethics requirements into actionable guidelines for IRB submissions, informed consent, and protected health information data handling.

What is the best way to assign ICMJE and CRediT authorship roles for a biomedical manuscript?▼

Assigning ICMJE and CRediT authorship roles for biomedical manuscripts involves mapping contributor tasks to standardized taxonomy roles, ensuring transparent attribution and compliant publication reporting.

How do I apply MeSH terminology and ICD coding when drafting medical research reports?▼

Applying MeSH terminology and ICD coding during medical research reporting standardizes disease and intervention vocabulary, ensuring compliant study design and accurate manuscript indexing.

Can I use this to ensure GDPR compliance for data handling in health services research?▼

Yes, you can use this to ensure GDPR compliance for data handling in health services research by integrating privacy regulation considerations into actionable data protection guidelines.

When do I need to include conflict of interest disclosure and trial registration for IRB review?▼

Conflict of interest disclosure and trial registration are required during IRB review preparation and publication planning to meet medical research compliance standards and ensure ethical study design.

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