Systematic literature review skill for clinical evaluation supporting regulatory submissions
Scanned 9/2/2026
Install to Claude Code
npx -y skills add a5c-ai/babysitter --skill clinical-literature-reviewer --agent claude-codeInstalls into .claude/skills of the current project.
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---
name: clinical-literature-reviewer
description: Systematic literature review skill for clinical evaluation supporting regulatory submissions
allowed-tools:
- Read
- Write
- Glob
- Grep
- Edit
- Bash
metadata:
specialization: biomedical-engineering
domain: science
category: Clinical Evidence
skill-id: BME-SK-023
graph:
domains: [domain:biomedical-engineering]
skillAreas: [skill-area:statistical-analysis, skill-area:data-analysis, skill-area:compliance-automation]
workflows: [workflow:experiment-design, workflow:peer-review-cycle]
roles: [role:biomedical-engineer, role:research-scientist]
---
# Clinical Literature Reviewer Skill
## Purpose
The Clinical Literature Reviewer Skill conducts systematic literature reviews for clinical evaluation, supporting medical device regulatory submissions with evidence synthesis per MEDDEV 2.7/1 and FDA guidance.
## Capabilities
- Literature search strategy development (PubMed, Embase, Cochrane)
- PICO framework application
- Abstract screening criteria
- Data extraction templates
- Appraisal of clinical data quality
- Evidence synthesis and summary tables
- MEDDEV 2.7/1 compliance checking
- Bias assessment tools
- Meta-analysis support
- Gap analysis for clinical evidence
- Ongoing literature surveillance
## Usage Guidelines
### When to Use
- Conducting clinical evidence reviews
- Supporting CER development
- Identifying evidence gaps
- Preparing regulatory submissions
### Prerequisites
- Clinical claims defined
- Search strategy approved
- Inclusion/exclusion criteria established
- Appraisal methodology selected
### Best Practices
- Document search methodology completely
- Apply consistent screening criteria
- Assess study quality systematically
- Synthesize evidence objectively
## Process Integration
This skill integrates with the following processes:
- Clinical Evaluation Report Development
- Clinical Study Design and Execution
- EU MDR Technical Documentation
- Post-Market Surveillance System Implementation
## Dependencies
- PubMed API
- Cochrane Library
- Embase database
- Systematic review tools
- Reference management software
## Configuration
```yaml
clinical-literature-reviewer:
databases:
- PubMed
- Embase
- Cochrane
- Web-of-Science
review-types:
- systematic
- scoping
- rapid
appraisal-tools:
- GRADE
- Oxford-CEBM
- Cochrane-RoB
```
## Output Artifacts
- Search strategies
- Screening logs
- Data extraction tables
- Quality appraisal forms
- Evidence synthesis reports
- PRISMA diagrams
- Summary of evidence tables
- Gap analysis reports
## Quality Criteria
- Search comprehensive and reproducible
- Screening criteria consistently applied
- Data extraction accurate
- Quality appraisal systematic
- Synthesis methodology appropriate
- Documentation meets MEDDEV 2.7/1
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