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Found 127 Skills
식약처 공공 OpenAPI를 k-skill-proxy 경유로 조회하기 전에 증상·복용상황을 반드시 되묻는 인터뷰형 의약품 안전 체크 스킬.
식약처/식품안전나라 공개 표면을 k-skill-proxy 경유로 조회하기 전에 증상·섭취상황을 반드시 되묻는 인터뷰형 식품 안전 체크 스킬.
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.
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.
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.
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.
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.
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.
Fast file finding using fd command-line tool with smart defaults, gitignore awareness, and parallel execution. Use when searching for files by name, extension, or pattern across directories.
Query openFDA API for drugs, devices, adverse events, recalls, regulatory submissions (510k, PMA), substance identification (UNII), for FDA regulatory data analysis and safety research.
Complete FDK management for macOS and Windows - install, upgrade, downgrade, and uninstall. Use when the user needs to install/configure/upgrade/downgrade/uninstall the Freshworks Development Kit, set up FDK on a new machine, asks about FDK installation on Mac or Windows, wants to change FDK version, or encounters FDK/CLI setup issues.
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.