The barcode layer of the visibility.cloud family, as offline verbs: resolve / verify / generate / serialize across GS1 (GTIN, element strings, Digital Link incl. compressed, GLN, SSCC), VIN, ISBN, FDA UDI, NDC and carrier tracking — plus an MCP door (reso

Official zero-dependency, high-speed JavaScript/TypeScript client for FDA & EU MDR Medical Device UDI Decoder

Universal Discovery Interface Toolkit

React implementation of the Universal Discovery Interface (UDI) chat — natural-language querying and visualization of biomedical datasets. Publishable as a library (`UDIChat` component) or as a standalone SPA.

Dette prosjektet inneholder UDI sitt interne designsystem, "Smudi". Les dokumentasjon om Bruken av Smudi og komponentene i [Storybook.](https://smudi.udi.no/)

FDA medical-device regulatory intelligence from keyless openFDA datasets.

Finds the lines the FDA gateway rejects in an SPL establishment registration, and how many days are left in the October 1 - December 31 window.

package for udi

FDA Regulations MCP — US Food & Drug Administration regulations (21 CFR).

Veterinary FDA MCP — openFDA Animal & Veterinary adverse events, pet/animal

Polyglot-v3 interface for node.js

Regulatory Catalysts MCP — high-value biotech regulatory calendar events (keyless).

FDA inspection outcomes, Form 483 observations, compliance actions and import refusals for drug, device and food establishments worldwide, from the FDA Data Dashboard (OII/ORA).

Release 28 of the FDA Nutrient Database for Standard Reference. Reference: US Department of Agriculture, Agricultural Research Service, Nutrient Data Laboratory. USDA National Nutrient Database for Standard Reference, Release 28. Version Current: Septemb

FDA drug data via openFDA: adverse-event reports and safety-signal tools (FAERS search, event counts, disproportionality/ROR-PRR summaries, reaction profiles, trends), drug and novel-drug approvals (Drugs@FDA, by-company application history), drug labelin

UDI package for utils purposes

为WEB端提供的公用UDI解析库 1、正常UDI码解析结果返回 2、异常UDI码AI解析返回结果

PDF Printer for FDA Portal

Classify FDA Warning Letters into structured regulatory data using TypeSafe's Jev (System One) model — selection over generation, so it never hallucinates a drug name.

OpenFDA Model Context Protocol