Capa Officer

Use when the user asks to write or draft a PhD / doctoral research proposal, research plan, 研究计划书, or 开题报告 — a forward-looking plan of background, gap, research questions, methodology, timeline, and significance, in English or Chinese. Triggers: "write a research proposal", "PhD proposal", "doctoral proposal", "研究计划书", "开题报告", "写博士研究计划". Not for backward-looking literature reviews / 综述 / surveys (use medical-imaging-review), nor grant forms bound to a funder's own template (国自然/NSF).

Use this skill when designing, generating an MVP blueprint for, auditing, refactoring, or explaining an agentic harness for any domain. Covers provider-neutral agent architecture for OpenAI, Anthropic, and OpenAI-compatible APIs: agent loops, tool design, permissions, system prompts, planning, goals, context compaction, memory, skills, MCP/external connectors, observability, evals, prompt caching, agent-legible environments, feedback loops, and safety.

When the user wants to plan PR, write a press release, or manage media relations. Also use when the user mentions "public relations," "PR," "press release," "media relations," "news release," "journalist," "media coverage," "product announcement," or "earned media." For on-site "As Seen In" or logos page, use press-coverage-page-generator.

When the user wants to launch on Product Hunt, prepare a PH submission, or plan launch day (hunter, first comment, timing, upvotes). Also use when the user mentions "Product Hunt," "launch on Product Hunt," "PH launch," "Product Hunt submission," "hunter," "Product of the Day," "upvotes," or "Product Hunt first comment." For multi-platform directory listings and paste-ready copy beyond PH, use directory-submission.

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.

Build a product-specific Amazon FBA prep, labeling, packing, and shipment-readiness plan. Use when a seller asks how to prepare units for FBA, choose barcode and labeling steps, plan poly-bagging, bubble wrap, sets, case packs, cartons, dangerous-goods review, supplier or prep-center instructions, or prevent receiving delays. Do not use as a substitute for current Seller Central requirements.