review
Analyze auto-memory for promotion candidates, stale entries, consolidation opportunities, and health metrics.
- License 许可
- MIT
- 最近更新
- 2026-03-13
- Stars
- ★ 4
- Forks
- 0
01 前言 Front Matter
- name
- review
- command
- /si:review
- description
- Analyze auto-memory for promotion candidates, stale entries, consolidation opportunities, and health metrics.
02 资源文件 1
- 参考文档package.json204 B
03 SKILL.md 正文
/si:review — Analyze Auto-Memory
Performs a comprehensive audit of Claude Code's auto-memory and produces actionable recommendations.
Usage
/si:review # Full review
/si:review --quick # Summary only (counts + top 3 candidates)
/si:review --stale # Focus on stale/outdated entries
/si:review --candidates # Show only promotion candidates
What It Does
Step 1: Locate memory directory
# Find the project's auto-memory directory
MEMORY_DIR="$HOME/.claude/projects/$(pwd | sed 's|/|%2F|g; s|%2F|/|; s|^/||')/memory"
# Fallback: check common path patterns
# ~/.claude/projects/<user>/<project>/memory/
# ~/.claude/projects/<absolute-path>/memory/
# List all memory files
ls -la "$MEMORY_DIR"/
If memory directory doesn't exist, report that auto-memory may be disabled. Suggest checking with /memory.
Step 2: Read and analyze MEMORY.md
Read the full MEMORY.md file. Count lines and check against the 200-line startup limit.
Analyze each entry for:
-
Recurrence indicators
- Same concept appears multiple times (different wording)
- References to "again" or "still" or "keeps happening"
- Similar entries across topic files
-
Staleness indicators
- References files that no longer exist (
findto verify) - Mentions outdated tools, versions, or commands
- Contradicts current CLAUDE.md rules
- References files that no longer exist (
-
Consolidation opportunities
- Multiple entries about the same topic (e.g., three lines about testing)
- Entries that could merge into one concise rule
-
Promotion candidates — entries that meet ALL criteria:
- Appeared in 2+ sessions (check wording patterns)
- Not project-specific trivia (broadly useful)
- Actionable (can be written as a concrete rule)
- Not already in CLAUDE.md or
.claude/rules/
Step 3: Read topic files
If MEMORY.md references or the directory contains additional files (debugging.md, patterns.md, etc.):
- Read each one
- Cross-reference with MEMORY.md for duplicates
- Check for entries that belong in the main file (high value) vs. topic files (details)
Step 4: Cross-reference with CLAUDE.md
Read the project's CLAUDE.md (if it exists) and compare:
- Are there MEMORY.md entries that duplicate CLAUDE.md rules? (→ remove from memory)
- Are there MEMORY.md entries that contradict CLAUDE.md? (→ flag conflict)
- Are there MEMORY.md patterns not yet in CLAUDE.md that should be? (→ promotion candidate)
Also check .claude/rules/ directory for existing scoped rules.
Step 5: Generate report
Output format:
? Auto-Memory Review
Memory Health:
MEMORY.md: {{lines}}/200 lines ({{percent}}%)
Topic files: {{count}} ({{names}})
CLAUDE.md: {{lines}} lines
Rules: {{count}} files in .claude/rules/
? Promotion Candidates ({{count}}):
1. "{{pattern}}" — seen {{n}}x, applies broadly
→ Suggest: {{target}} (CLAUDE.md / .claude/rules/{{name}}.md)
2. ...
?️ Stale Entries ({{count}}):
1. Line {{n}}: "{{entry}}" — {{reason}}
2. ...
? Consolidation ({{count}} groups):
1. Lines {{a}}, {{b}}, {{c}} all about {{topic}} → merge into 1 entry
2. ...
⚠️ Conflicts ({{count}}):
1. MEMORY.md line {{n}} contradicts CLAUDE.md: {{detail}}
? Recommendations:
- {{actionable suggestion}}
- {{actionable suggestion}}
When to Use
- After completing a major feature or debugging session
- When
/si:statusshows MEMORY.md is over 150 lines - Weekly during active development
- Before starting a new project phase
- After onboarding a new team member (review what Claude learned)
Tips
- Run
/si:review --quickfrequently (low overhead) - Full review is most valuable when MEMORY.md is getting crowded
- Act on promotion candidates promptly — they're proven patterns
- Don't hesitate to delete stale entries — auto-memory will re-learn if needed
04 同仓库更多 Skills
risk-management-specialist
Medical device risk management specialist implementing ISO 14971 throughout product lifecycle. Provides risk analysis, risk evaluation, risk control, and post-production information analysis. Use when user mentions risk management, ISO 14971, risk analysis, FMEA, fault tree analysis, hazard identification, risk control, risk matrix, benefit-risk analysis, residual risk, risk acceptability, or post-market risk.
regulatory-affairs-head
Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathways for new medical devices; drafts responses to FDA deficiency letters and Notified Body queries; develops CE marking technical documentation under EU MDR 2017/745; coordinates multi-market approval strategies across FDA, EU, Health Canada, PMDA, and NMPA; and maintains regulatory intelligence on evolving standards. Use when users need to plan or execute FDA submissions, navigate 510(k) or PMA approval processes, achieve CE marking, prepare pre-submission meeting materials, write regulatory strategy documents, respond to agency queries, or manage compliance documentation for medical device market access.
quality-manager-qms-iso13485
ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support. Use when working with medical device quality systems, preparing for ISO 13485 audits, managing regulatory compliance documentation, setting up corrective actions, or building audit preparation programs. Useful for quality management, audit preparation, regulatory compliance, medical device documentation, and corrective action workflows.
quality-manager-qmr
Senior Quality Manager Responsible Person (QMR) for HealthTech and MedTech companies. Provides quality system governance, management review leadership, regulatory compliance oversight, and quality performance monitoring per ISO 13485 Clause 5.5.2.
quality-documentation-manager
Document control system management for medical device QMS. Covers document numbering, version control, change management, and 21 CFR Part 11 compliance. Use for document control procedures, change control workflow, document numbering, version management, electronic signature compliance, or regulatory documentation review.
qms-audit-expert
ISO 13485 internal audit expertise for medical device QMS. Covers audit planning, execution, nonconformity classification, and CAPA verification. Use for internal audit planning, audit execution, finding classification, external audit preparation, or audit program management.