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Found 142 Skills
Run the participant-facing CTFd CLI directly from its Git repository with uvx. Use when an agent needs to list or inspect CTFd challenges, view hints or the scoreboard, inspect the current user's solves and submissions, submit a flag, or unlock a hint without installing the ctfd package globally.
Use when invoked by cfd-bioreactor orchestrator to provide adversarial engineering review of CFD simulation plans and generated code. Challenges mesh quality, boundary conditions, solver parameters, stabilization choices, and physical plausibility. Produces severity-rated review with approval status.
식약처/식품안전나라 공개 표면을 k-skill-proxy 경유로 조회하기 전에 증상·섭취상황을 반드시 되묻는 인터뷰형 식품 안전 체크 스킬.
식약처 공공 OpenAPI를 k-skill-proxy 경유로 조회하기 전에 증상·복용상황을 반드시 되묻는 인터뷰형 의약품 안전 체크 스킬.
Query, search, and download data from the openFDA API for drugs, devices, foods, tobacco, cosmetics, animal and veterinary products, substances, and transparency data. Use for FDA adverse events, recalls, labeling, approvals, shortages, 510(k) clearances, NDC lookups, and any FDA safety or regulatory data query across all 28 API endpoints.
Work with NFDomains (NFDs), the Algorand Name Service (.algo domains), using the @txnlab/nfd-sdk TypeScript SDK. Use when building features that involve resolving .algo domain names to addresses (or reverse), displaying NFD avatars and metadata, searching for NFDs, minting new NFDs, purchasing NFDs from the marketplace, managing NFD metadata and linked addresses, working with NFD segments (subdomains), interacting with NFD vaults, or integrating NFD name resolution into Algorand applications.
James Bach's HTSM Product Factors (SFDIPOT) analysis for comprehensive test strategy generation. Use when analyzing requirements, epics, or user stories to generate prioritized test ideas across Structure, Function, Data, Interfaces, Platform, Operations, and Time dimensions.
Use when a user mentions Jupiter token verification, VRFD eligibility, paying 1000 JUP to verify a token, submitting a verification request, or updating metadata via the Jupiter express verification flow.
Senior FDA consultant and specialist for medical device companies including HIPAA compliance and requirement management. Provides FDA pathway expertise, QSR compliance, cybersecurity guidance, and regulatory submission support. Use for FDA submission planning, QSR compliance assessments, HIPAA evaluations, and FDA regulatory strategy development.
Query openFDA API for drugs, devices, adverse events, recalls, regulatory submissions (510k, PMA), substance identification (UNII), for FDA regulatory data analysis and safety research.
FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QSR (21 CFR 820) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QSR, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.
Provides domain knowledge and guidance for the Flare Data Connector (FDC)—attestation types, request flow, Merkle proofs, verifier/DA Layer, and smart contract integration. Use when working with FDC, cross-chain attestations, EVMTransaction, Web2Json, Payment, AddressValidity, XRPPayment, XRPPaymentNonexistence, proof-of-reserves, weather insurance, or Flare Developer Hub FDC guides and starter repos.