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日本語の概要は準備中です。原文の説明を表示しています。
aibot88/sec_skill_store42026年5月27日 更新
無料GitHub で公開
adverse-event-reporter
Adverse event monitoring and reporting skill for MDR/MEDWATCH compliance
含まれるファイル（2）
- SKILL.md2.4 KB
- source.json616 B
SKILL.md（原文）
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Adverse Event Reporter Skill
Purpose
The Adverse Event Reporter Skill supports adverse event monitoring and regulatory reporting for medical devices, ensuring compliance with FDA MDR requirements and EU vigilance obligations.
Capabilities
- MDR reportability assessment
- FDA Form 3500A population assistance
- MEDWATCH submission guidance
- EU vigilance reporting templates
- Trend analysis and signal detection
- PSUR data compilation
- Field safety corrective action templates
- Complaint coding (MedDRA)
- Risk assessment updates
- Corrective action tracking
- Regulatory notification timelines
Usage Guidelines
When to Use
- Assessing adverse event reportability
- Preparing regulatory reports
- Conducting trend analyses
- Managing field actions
Prerequisites
- Complaint information received
- Investigation completed
- Device information available
- Regulatory requirements identified
Best Practices
- Assess reportability promptly
- Document decision rationale
- Track reporting timelines
- Integrate with risk management
Process Integration
This skill integrates with the following processes:
- Post-Market Surveillance System Implementation
- Clinical Evaluation Report Development
- Medical Device Risk Management (ISO 14971)
- EU MDR Technical Documentation
Dependencies
- FDA MAUDE database
- EUDAMED system
- MedDRA coding dictionary
- Complaint management systems
- Risk management databases
Configuration
adverse-event-reporter:
reporting-systems:
- FDA-MDR
- EU-vigilance
- Health-Canada
- TGA
report-types:
- death
- serious-injury
- malfunction
- field-safety-corrective-action
timelines:
- 30-day
- 5-day
- annual
Output Artifacts
- Reportability assessments
- FDA Form 3500A drafts
- EU vigilance reports
- Trend analysis reports
- PSUR contributions
- FSCA notifications
- Risk management updates
- Corrective action plans
Quality Criteria
- Reportability assessed per regulations
- Reports submitted within timelines
- MedDRA coding accurate
- Trend analysis comprehensive
- Risk management updated
- Documentation audit-ready
レビュー
まだレビューはありません。使ってみた感想をお寄せください。
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日本語の概要は準備中です。原文の説明を表示しています。
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aibot88/sec_skill_store42026年5月27日 更新