roadmap-communicator
Use when preparing roadmap narratives, release notes, changelogs, or stakeholder updates tailored for executives, engineering teams, and customers.
- License 许可
- MIT
- 最近更新
- 2026-03-18
- Stars
- ★ 39
- Forks
- 10
01 前言 Front Matter
- name
- roadmap-communicator
- description
- Use when preparing roadmap narratives, release notes, changelogs, or stakeholder updates tailored for executives, engineering teams, and customers.
02 资源文件 3
- 参考文档references/communication-templates.md961 B
- 参考文档references/roadmap-templates.md1.0 KB
- 脚本scripts/changelog_generator.py4.9 KB
03 SKILL.md 正文
Roadmap Communicator
Create clear roadmap communication artifacts for internal and external stakeholders.
When To Use
Use this skill for:
- Building roadmap presentations in different formats
- Writing stakeholder updates (board, engineering, customers)
- Producing release notes (user-facing and internal)
- Generating changelogs from git history
- Structuring feature announcements
Roadmap Formats
- Now / Next / Later
- Best for uncertainty and strategic flexibility.
- Communicate direction without false precision.
- Timeline roadmap
- Best for fixed-date commitments and launch coordination.
- Requires active risk and dependency management.
- Theme-based roadmap
- Best for outcome-led planning and cross-team alignment.
- Groups initiatives by problem space or strategic objective.
See references/roadmap-templates.md for templates.
Stakeholder Update Patterns
Board / Executive
- Outcome and risk oriented
- Focus on progress against strategic goals
- Highlight trade-offs and required decisions
Engineering
- Scope, dependencies, and sequencing clarity
- Status, blockers, and resourcing implications
Customers
- Value narrative and timing window
- What is available now vs upcoming
- Clear expectation setting
See references/communication-templates.md for reusable templates.
Release Notes Guidance
User-Facing Release Notes
- Lead with user value, not internal implementation details.
- Group by workflows or user jobs.
- Include migration/behavior changes explicitly.
Internal Release Notes
- Include technical details, operational impact, and known issues.
- Capture rollout plan, rollback criteria, and monitoring notes.
Changelog Generation
Use:
python3 scripts/changelog_generator.py --from v1.0.0 --to HEAD
Features:
- Reads git log range
- Parses conventional commit prefixes
- Groups entries by type (
feat,fix,chore, etc.) - Outputs markdown or plain text
Feature Announcement Framework
- Problem context
- What changed
- Why it matters
- Who benefits most
- How to get started
- Call to action and feedback channel
Communication Quality Checklist
- [ ] Audience-specific framing is explicit.
- [ ] Outcomes and trade-offs are clear.
- [ ] Terminology is consistent across artifacts.
- [ ] Risks and dependencies are not hidden.
- [ ] Next actions and owners are specified.
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.