Pharmacy Practice Bundle | Prompeteer.ai

Included Skills (45)

1. Gemini API — Use when the user asks about using Gemini in an enterprise environment or explicitly mentions Vertex AI, Google Cloud, or Agent Platform. Guides the usage of the Gemini API on Agent Platform with the Google Gen AI SDK. Covers SDK usage (Python, JS/TS, Go, Java, C#), capabilities like multimodal inputs, tools, media generation, caching, batch prediction, and Live API.
2. Algorithmic Art — Creating algorithmic art using p5.js with seeded randomness and interactive parameter exploration. Use this when users request creating art using code, generative art, algorithmic art, flow fields, or particle systems. Create original algorithmic art rather than copying existing artists' work to avoid copyright violations.
3. Command Development — This skill should be used when the user asks to "create a slash command", "add a command", "write a custom command", "define command arguments", "use command frontmatter", "organize commands", "create command with file references", "interactive command", "use AskUserQuestion in command", or needs guidance on slash command structure, YAML frontmatter fields, dynamic arguments, bash execution in commands, user interaction patterns, or command development best practices for Claude Code.
4. Hookify Rule Writer — This skill helps users create and configure Hookify rules for customizing agent behavior based on defined patterns and events.
5. Hookify Rule Creator — This skill helps users create and configure Hookify rules for pattern matching and message display within the agent's workflow.
6. Hookify Rule Writer — This skill helps users create and configure Hookify rules for customizing agent behavior based on defined patterns and events.
7. Skill Development Guide — This skill guides users in creating, improving, and organizing skills for Claude Code plugins, ensuring effective and modular agent capabilities.
8. GSAP ScrollTrigger Helper — This skill assists developers using GSAP's ScrollTrigger plugin to create scroll-linked animations, parallax effects, and pinned sections in web projects.
9. Opencli Browser — Use when an agent needs to drive a real Chrome window via opencli — inspect a page, fill forms, click through logged-in flows, or extract data ad-hoc. Covers the selector-first target contract, compound form fields, stale-ref handling, network capture, and the agent-native envelopes the CLI returns. Not for writing adapters — see opencli-adapter-author for that.
10. Add Provider Package — Guide for adding new AI provider packages to the AI SDK. Use when creating a new @ai-sdk/<provider> package to integrate an AI service into the SDK.
11. MCPB Package Builder — This skill packages a local MCP server with its runtime, creating a single installable file for distribution to users without Node/Python.
12. Opencli Autofix — Automatically fix broken OpenCLI adapters when commands fail. Load this skill when an opencli command fails — it guides you through collecting a trace artifact, patching the adapter, retrying, and filing an upstream GitHub issue after a verified fix. Works with any AI agent.
13. Opencli Browser — Use when an agent needs to drive a real Chrome window via opencli — inspect a page, fill forms, click through logged-in flows, or extract data ad-hoc. Covers the selector-first target contract, compound form fields, stale-ref handling, network capture, and the agent-native envelopes the CLI returns. Not for writing adapters — see opencli-adapter-author for that.
14. Add Harness Package — Guide for adding new AI SDK harness packages. Use when creating a new @ai-sdk/harness-<name> package that adapts a coding-agent runtime to HarnessV1.
15. Provider Package Integration — This skill guides developers in creating new provider packages for the AI SDK, enabling integration of various AI services.
16. Project Artifact — Generate and publish a project status artifact — an opinionated, tabbed status page for a project too big for one update (overview & success criteria, the workstream sequence, next steps, plus background, plan, risks & open questions, and decisions/FAQ when they earn a tab) — published with the built-in Artifact tool to a default-private claude.ai page the user can share with teammates. Use when a piece of work spans several workstreams and you want a shareable overview kept current. Each artifact is backed by a small per-project config in the plugin data dir, so refreshing it re-gathers live state, redeploys the same URL, and reports only the delta. For software projects whose workstreams are PRs, also read swe.md (the X.Y PR-numbering convention; pulling PR state with gh/git; a per-PR detail block). Needs the built-in Artifact tool (claude.ai login). Not for single-PR changes or public docs.
17. Partnerships Architect — Use when a startup is approached by a prospective partner and someone has to decide should we sign this partner, at what partner tier (referral / reseller / OEM / SI-consulting / strategic alliance), with what joint GTM commitment, and at what revshare. Classifies partner tier from independent-demand evidence vs. preferential-terms hunting, designs a 90-day joint GTM plan, models revshare against direct-sale margin, and surfaces kill criteria for unwinding under-performing partnerships. For Head of Partnerships, Head of BD, and Founder-CEOs doing reseller agreement, OEM deal, or strategic alliance review — not technical sale enablement, not channel cost economics, not M&A.
18. CCPA Compliance Assistant — Helps businesses comply with CCPA/CPRA by implementing data privacy features and responding to consumer data requests.
19. 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.
20. HIPAA Compliance Implementation — This skill helps developers implement HIPAA compliance in healthcare applications, covering PHI handling, encryption, audit logging, and access controls.
21. Business Proposal Generator — Crafts persuasive business proposals, including scope, timelines, and pricing, to help users win deals and partnerships.
22. PCI DSS Compliance — Achieve PCI DSS compliance by scoping, implementing controls, and selecting SAQ types for secure payment card data handling.
23. SOC2 Compliance Assistant — Helps SaaS companies achieve SOC 2 Type II compliance by implementing controls and preparing for audits to meet enterprise requirements.
24. Referral Program — When the user wants to design, launch, or optimize a referral or affiliate program. Use when they mention 'referral program,' 'affiliate program,' 'word of mouth,' 'refer a friend,' 'incentive program,' 'customer referrals,' 'brand ambassador,' 'partner program,' 'referral link,' or 'growth through referrals.' Covers program mechanics, incentive design, and optimization — not just the idea of referrals but the actual system.
25. Fda Consultant Specialist — FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QMSR (21 CFR 820, which incorporates ISO 13485:2016 by reference since 2026-02-02; formerly QSR) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QMSR, QSR, ISO 13485 for FDA, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.
26. Compliance Os — Compliance OS — meta-orchestrator that lets compliance teams CONFIGURE which frameworks apply, COMPUTE cross-framework control overlap, SIMULATE internal audits, and CONSOLIDATE evidence across multiple frameworks. Four decisions: (1) Given a company profile, which of the 12 supported frameworks apply (ISO 27001/13485/42001/14971, EU AI Act, MDR 745, GDPR, SOC 2, FDA QSR, NIST CSF 2.0, NIS2, HIPAA)? (2) Across selected frameworks, which controls overlap and how much evidence reuses? (3) For a given framework + scope, what does a realistic mock audit produce — drawing from the 205-scenario library? (4) Across selected frameworks, what's the unified evidence checklist with reuse map? Use when standing up a multi-framework program, planning the annual audit calendar, or preparing for certification stage 1. Does NOT replace per-framework skills (it orchestrates them).
27. Gdpr Dsgvo Expert — GDPR and German DSGVO compliance automation. Scans codebases for privacy risks, generates DPIA documentation, tracks data subject rights requests with Art. 12(3) one-month deadlines. Use when running GDPR compliance assessments, privacy audits, data protection planning, DPIA generation, or data subject rights (DSAR) management (e.g., 'check this service for GDPR risks', 'track an access request deadline'). Final compliance determinations route to the DPO or legal counsel.
28. Information Security Manager Iso27001 — ISO 27001 ISMS implementation and cybersecurity governance for HealthTech and MedTech companies. Use when designing an ISMS, running security risk assessments, implementing controls, pursuing ISO 27001 certification, preparing security audits, responding to security incidents, or verifying compliance. Covers ISO 27001, ISO 27002, healthcare security, and medical device cybersecurity.
29. Mdr 745 Specialist — EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, Art. 86 PSUR schedules, and EUDAMED integration. Use when classifying a medical device under MDR, building or gap-checking a technical file, planning clinical evaluation or PMS/PSUR cadence, or preparing for notified body review (e.g., 'what class is my device under MDR', 'review my PSUR schedule').
30. 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 when working on document control procedures, change control workflows, document numbering, version management, electronic signature compliance, or regulatory documentation review.
31. 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. Use when leading management reviews, setting quality policy and objectives, monitoring quality KPIs and cost of quality, or exercising QMR governance and regulatory oversight responsibilities.
32. Senior Secops — Senior SecOps engineer skill for application security, vulnerability management, compliance verification, and secure development practices. Runs SAST/DAST scans, generates CVE remediation plans, checks dependency vulnerabilities, creates security policies, enforces secure coding patterns, and automates compliance checks against SOC2, PCI-DSS, HIPAA, and GDPR. Use when conducting a security review or audit, responding to a CVE or security incident, hardening infrastructure, implementing authentication or secrets management, running penetration test prep, checking OWASP Top 10 exposure, or enforcing security controls in CI/CD pipelines.
33. Parallel Agent Orchestrator — Spawns parallel AI agents in isolated git worktrees to collaboratively solve tasks, ideal for code optimization and research exploration.
34. Eu AI Act Specialist — EU AI Act (Regulation (EU) 2024/1689) operational compliance for compliance teams. Three Article-level decisions: (1) What's the risk tier of this AI system — prohibited (Art. 5), high-risk (Art. 6 + Annex III), limited-risk (Art. 50), or minimal-risk? (2) For high-risk systems, what's the Article 43 conformity assessment route (Module A internal control vs Module H full QMS + notified body) and what goes in the Annex IV technical documentation? (3) Per organizational role (provider / deployer / importer / distributor / authorized representative), what are the active obligations and deadlines? Use during AI system intake review, when planning conformity assessment, or when scoping deployer obligations. Cites Articles + Annexes for every output. NOT executive AI strategy (see chief-ai-officer-advisor). NOT a legal substitute.
35. Eu AI Act Specialist — EU AI Act (Regulation (EU) 2024/1689) operational compliance for compliance teams. Three Article-level decisions: (1) What's the risk tier of this AI system — prohibited (Art. 5), high-risk (Art. 6 + Annex III), limited-risk (Art. 50), or minimal-risk? (2) For high-risk systems, what's the Article 43 conformity assessment route (Module A internal control vs Module H full QMS + notified body) and what goes in the Annex IV technical documentation? (3) Per organizational role (provider / deployer / importer / distributor / authorized representative), what are the active obligations and deadlines? Use during AI system intake review, when planning conformity assessment, or when scoping deployer obligations. Cites Articles + Annexes for every output. NOT executive AI strategy (see chief-ai-officer-advisor). NOT a legal substitute.
36. Capacity Planner — Use when an ops leader (Director of CX, Head of Support, VP Ops, Head of BizOps, Head of IT ops, Head of Finance ops) is sizing ops capacity, building a headcount plan, modeling utilization risk, planning Q3 capacity or annual support capacity, or designing CS coverage — and needs Erlang-C queueing math, P90 demand sizing, shrinkage-adjusted FTE, manager-trigger thresholds, and a quarterly hiring sequence with ramp + attrition. Apply when sustained team utilization is above 80% or when the team is growing >50% in 12 months. Run before committing the headcount budget. This is NOT engineering capacity (see vpe-advisor for DORA + cycle time) and NOT strategic 3-year workforce planning (see chro-advisor).
37. Agent Design Patterns — Provides design patterns for developers building autonomous coding agents, enabling efficient and reliable AI-driven automation workflows.
38. Karpathy AI Simulator — Simulates Andrej Karpathy, providing deep learning expertise and educational insights for users interested in AI and neural networks.
39. Angular UI Guidance — Offers Angular UI patterns for loading, errors, and data, assisting developers in building robust UI components.
40. Angular UI Guidance — Offers Angular UI patterns for loading, errors, and data, streamlining UI component creation and state management.
41. Agent Architecture Patterns — Provides proven design patterns for developers to build robust and efficient autonomous coding agents with tool-calling capabilities.
42. ActiveCampaign Task Automation — Automate ActiveCampaign CRM tasks like contact management and automation enrollment, streamlining workflows for marketing and sales professionals.
43. Karpathy AI Simulator — Emulates Andrej Karpathy, offering deep learning expertise and educational insights for users seeking AI knowledge and practical guidance.
44. Checkov Security Scanner — This skill provides expert guidance for using Checkov to scan infrastructure-as-code for security misconfigurations and compliance violations, aiding developers.
45. Azure OpenAI Service — This skill provides access to OpenAI models on Azure, offering enterprise compliance and Azure-native authentication for developers and organizations.