AI/ML medical device validation skill implementing FDA's GMLP principles
Scanned 9/2/2026
Install to Claude Code
npx -y skills add a5c-ai/babysitter --skill aiml-validation-framework --agent claude-codeInstalls into .claude/skills of the current project.
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---
name: aiml-validation-framework
description: AI/ML medical device validation skill implementing FDA's GMLP principles
allowed-tools:
- Read
- Write
- Glob
- Grep
- Edit
- Bash
metadata:
specialization: biomedical-engineering
domain: science
category: Medical Device Software
skill-id: BME-SK-021
graph:
domains: [domain:biomedical-engineering]
skillAreas: [skill-area:machine-learning-frameworks, skill-area:statistical-analysis, skill-area:compliance-automation]
workflows: [workflow:experiment-design, workflow:peer-review-cycle]
roles: [role:biomedical-engineer, role:ml-engineer]
---
# AI/ML Validation Framework Skill
## Purpose
The AI/ML Validation Framework Skill supports validation of AI/ML-enabled medical devices per FDA Good Machine Learning Practice (GMLP) principles, addressing data quality, model performance, and predetermined change control.
## Capabilities
- Training data quality assessment
- Ground truth labeling validation
- Model performance metrics calculation (AUC, sensitivity, specificity)
- Subgroup performance analysis
- Bias and fairness evaluation
- Predetermined change control plan (PCCP) templates
- Clinical validation study design
- Locked algorithm vs. adaptive documentation
- Model explainability documentation
- Performance monitoring planning
- Real-world performance tracking
## Usage Guidelines
### When to Use
- Validating AI/ML algorithms
- Assessing training data quality
- Planning clinical validation studies
- Preparing FDA AI/ML submissions
### Prerequisites
- Algorithm development complete
- Training/test datasets curated
- Ground truth established
- Intended use clearly defined
### Best Practices
- Document data management practices
- Validate on diverse populations
- Plan for performance monitoring
- Consider predetermined change control
## Process Integration
This skill integrates with the following processes:
- AI/ML Medical Device Development
- Software Verification and Validation
- Clinical Evaluation Report Development
- Post-Market Surveillance System Implementation
## Dependencies
- FDA AI/ML guidance
- GMLP principles
- Fairness toolkits (AIF360, Fairlearn)
- Statistical analysis tools
- Clinical study resources
## Configuration
```yaml
aiml-validation-framework:
algorithm-types:
- locked
- adaptive
- continuously-learning
performance-metrics:
- AUC
- sensitivity
- specificity
- PPV
- NPV
subgroup-categories:
- age
- sex
- race
- disease-severity
```
## Output Artifacts
- Data management documentation
- Algorithm description documents
- Performance reports
- Bias/fairness assessments
- PCCP documents
- Clinical validation protocols
- Monitoring plans
- FDA submission sections
## Quality Criteria
- Training data quality documented
- Ground truth methodology validated
- Performance meets clinical requirements
- Subgroup performance acceptable
- Bias assessments completed
- PCCP appropriate for algorithm type
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