Track competitors while you build your plugin.

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Connect ChatGPT to your Datasite virtual data room - the secure workspace where thousands of M&A deals are facilitated annually. Set up folder structures, invite users, search documents, track buyer Q&A, and audit data room… …h documents semantically - "Search the data room for any documents related to pending litigation or regulatory risk." 3. Track buyer Q&A - "Show me all open Q&A questions in the data room and draft responses where we have supporting documents." 4. Audit deal room readiness - "Check the data room for…

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Search millions of Australian court, tribunal, regulatory, and other government records that are or were publicly available and have been indexed by DATAV3. Find records by name, topic, ABN or ACN, narrow results by source and date, and retrieve the available documents and details behind a match. A DATAV3 account is required.

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Dovetail Regulatory connects medtech teams to their Dovetail workspace from ChatGPT. Users can inspect devices and tasks, search and edit regulatory documents and data keys, manage traceability links and comments, research standards and FDA 510(k)s, recall project knowledge, and run regulatory research and review agents.

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Connect ChatGPT to Twelve Data for current and historical market information. Look up prices, time series, technical indicators, company fundamentals, earnings, dividends, market movers, analyst data, regulatory filings, and reference data for stocks, ETFs, mutual funds, forex, crypto, and commodities. Users authenticate with their own Twelve Data account, so available data and rate limits follow t…

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Search medical-device data

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…legal and compliance teams. You build a compliance profile once — jurisdictions, sector, headcount, data and AI exposure, supply chain, materiality thresholds — and each scan queries US federal, optionally selected US states, EU, and UK primary sources for what has changed since your last run, suppr… …memo, a client alert, obligation register rows, a short digest, and a forward compliance calendar. Regulatory intelligence, not legal advice.

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Check data against the standards, canonical models and policies it claims to conform to, and get back a graded, machine-readable result that says what was checked, what was not, and why. dVeracity is a veri… …icy guardrails), validate a payload against a named standard before submitting it, look up approved regulatory compliance policies with their rules and provenance, and query verified datasets in natural language. Every result states its model version and the checks it ran, so it can be handed to a r…

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Explore data and information about Brazil’s electric power sector with Index Energia. Access prices, market data, system operations, generation, load, hydrology, reservoirs, curtailment, CCEE data, regulatory documents, Brazilian Official Gazette publications, and structured analyses in one place. DEX skills add workflows for monitoring the energy market, preparing recurring briefings and config…

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Use the PolicyNote app to access structured policy and regulatory intelligence from around the world. Search legislation, regulatory actions, policy updates, and government activity across jurisdictions. The app enables developers, analysts, and policy professionals to retrieve policy data programmatically and integrate it into internal tools, research workflows, dashboards, or monitoring systems. Queries return structured information about policy developments, government sources,…

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…emory cio-autonomy-map truth-gap human-control shadow-agenda steering-pack decision-sla vendor-exit regulatory-shock capital-allocation cio-os-maturity stakeholder-alignment exception-waiver policy-as-code benefits-realization escalation-drafts control-tower data-trust architecture-runway executive-narrative decision-backlog due-diligence resilience customer-trust ai-portfolio cost-of-delay decision-rights okr-strategy risk-acceptance service-health depen…

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FDA FDA records FDA database openFDA Drugs@FDA FDA approvals drug approvals warning letters FDA warning letters complete response letters CRL Form 483 FDA inspections import refusals enforcement reports drug labels packa… …rials.gov PubMed Europe PMC literature search systematic reviews citation counts open access papers regulatory regulatory affairs regulatory intelligence life sciences pharma biotech medical affairs quality assurance drug development meta-analysis medication drug information public health biomedical…

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public records regulatory data sec fda sanctions compliance due diligence open data mcp morvs

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…qPCR master mix and plate map. • Practical guides on protocols and SOPs, lab notebooks, inventory, data integrity and GLP, and equipment records, with links to cite. Privacy: tool inputs are used only to compute the answer and are not stored. No sign-in is required. Limitations: results are calculation and documentation aids, not scientific, safety or regulatory advice; scientists should check values against their own lab's requirements. Molecular weights and stock concentrations come from the user. The reagent label tool reads label text, not imag…

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Ask about insurance carriers, products and regulatory filings, and get answers backed by the filings and source documents in Effective. With the Effective plugin you can: - Find competitors' rate, rule and form filings for a line of business a… …ffective changes apart. - Review the actuarial support for a rate change: assumptions, exhibits and data gaps. - Compare coverage wording, exclusions, endorsements and form editions across filings. - Benchmark a carrier's premium and underwriting results from its annual financials. - Create and upda…

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…ials, with a ranked list of suppliers. Every FDA result states the query it ran and the date of the data. Quotes are estimates from a cost model, not supplier prices. For engineering, regulatory and sourcing work; not medical advice.

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…ual property and digital assets; financial and tax organization; commercial agreements, privacy and regulatory records; disputes and investigations; and data-room organization. Get a provisional process-readiness score alongside assessment completeness and reviewed-evidence coverage, so the result shows both your preparation and the limits of the info…

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Tap into NyquistAI's comprehensive database of FDA medical device intelligence, including all 510(k), PMA, De Novo, and HDE clearances and approvals, adverse events, recalls, guidance, and more. This app provides FDA regulatory and safety intelligence for research, compliance, and monitoring purposes only. It does not provide medical advice or clinical recommendations.

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…r comment period final rules effective date federal register notices by agency track proposed rules regulatory digest

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…n teams to their Atlas workspace. Search suppliers and certification records, find trade and tariff data, review organization documents, and access published market intelligence reports. Use available Atlas tools to manage supplier and shipment records, verification workflows, paperwork, signatures,… …ation results and AI-generated research support due diligence; they do not guarantee certification, regulatory compliance, or customs clearance.

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…tion against the FDA reference values in 21 CFR 101. Add custom ingredients with your own nutrition data, set serving sizes, and export the Nutrition Facts label. Every recipe is versioned: reformulate freely, then see which ingredient change moved which nutrient, and which version any given label c… …where a number came from without reconstructing it. For food manufacturers, co-packers, and R&D and regulatory teams working on packaged food sold in the United States.

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Search Digital Policy Alert for regulatory developments affecting the digital economy, including AI governance, data protection, content moderation and digital taxation. Find implementing jurisdictions, policy details, implementation dates, and links to the underlying records and official sources.

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Independent, unofficial app developed by James Jenrette / 1102tools using public data from the Electronic Code of Federal Regulations (eCFR). This app is not affiliated with or endorsed by the U.S. government. Search codified federal regulations, retrieve FAR and DFARS text, inspect regulatory structure, and compare historical versions through 13 read-only tools. Results identify the available source date. The app provides source text and does not determine which rules govern a s…

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…rket: a Breakout Watch / catalyst radar of upcoming market-moving events — drug-approval decisions, regulatory and enforcement actions, appropriations and contract deadlines, executive orders and policy shifts — each with a breakout score and expected-impact scenarios, plus prediction-market odds an… …is available; upgrade for full unmasked signals, the Alpha Score, catalyst radar, and alerts). All data is derived from public records and is informational only — not investment advice.

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Gosset gives biopharma business-development, strategy and investment teams a curated database of drugs, clinical trials, companies, deals, news and regulatory events. In ChatGPT you can search drug pipelines by target, disease, modality or developer; find and compare clinical trials; look up licensing and M&A deals; estimate a trial's probability…

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…al name, and get one plain explanation of what it is, what it does and who says so. The EU's CosIng database supplies cosmetic functions and short definitions of what an ingredient is, and ChEBI supplies chemical roles. Paula's Choice and NIVEA, skincare brands, and INKEEDecoder, an editorial ingred… …treated as other names for it. HelloGem doesn't give safety, medical, concentration, formulation or regulatory advice. Each answer has a Report an issue link tied to the exact HelloGem result. If the problem is in how ChatGPT worded it, paste that part. Tool requests and results are stored privately…

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…business, and this app will: • Assess your cyber risk profile • Identify relevant cover (including data breach response, ransomware, business interruption, cyber extortion, and regulatory defence) • Generate tailored UK cyber insurance quotes • Outline key limits, excesses, and optional extensions • Highlight risk management considerations that may impact pricing Once you’re…

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Chemical safety data for lab work, cited to supplier SDS: compatibility, hazards, PPE, storage, disposal, exposure limits, transport and regulatory lists.

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…tions. Distances, durations, emissions and cost bands are planning estimates from published network data and stated assumptions — an overview, not navigational advice, and not a freight quote. It does not report live vessel positions, schedules or tracking; it does not plan passenger travel; it gives no customs, tariff or regulatory guidance; and it books nothing. It will not invent a UN/LOCODE: a place the catalog cannot identify comes back as a question with suggestions rather than a guess. No account or sign-in is n…

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Search Australian study and skilled-migration data from One U Education (www.oneuedu.com). Find about 50,000 CRICOS-registered courses by location, qualification level, field of study, tuition, English requirements and course length, with yearly… …d private colleges, and Registered Training Organisations (RTOs) with their registration status and regulatory decisions. Explore ANZSCO skilled occupations with their lists, visa options, skills assessment rules and labour agreements; the SkillSelect EOI pool, subclass 189 invitation rounds and an…

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…ion programme (schedule), procurement and deliveries, the action and issue worklist, and authority (regulatory) submissions. - Search the drawing register and contract clauses. - Search your firm library, licensed standards and building codes. Every answer cites the Ordinate records behind it and st… …that explains why. Limitations: all tools are read-only. The plugin cannot create, change or delete data in Ordinate, send email, or approve or submit anything. It reads message text, not email attachments, unless the same file is also filed as a project document.

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Rhizome's built an AI regulatory coworker that helps life sciences know what their regulator thinks. We're backed by the same investors as Benchling and have gone from 0 -> >25 customers in the last 18 months. We've indexed >3 TB worth of data put out by the FDA, EMA, MHRA, PMDA, etc., and built an agent that helps you: - automate precedents research - research FDA expectations around clinical endpoints, trial design, labeling, etc. -…

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…tes in the UAE; cross-border structuring; dispute resolution; legal drafting and documentation; and regulatory compliance and licensing. It also covers who the firm serves, its office hours and logistics in Fujairah, and accessibility information. The connector exposes two read-only tools. search re… …al source URL, and a text snippet. fetch returns a document's full text, its canonical URL, and metadata. Every result resolves to the exact page it came from, so answers stay grounded and citable to source. All content is public business information describing the firm's services. It is general inf…

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…T. Connect to your Sumsub account to onboard applicants, generate verification links, and pull live data on identities, businesses, transactions, AML screening cases, and fraud networks—all in plain language. Triage your review queue by risk, assemble due-diligence dossiers, investigate suspicious activity, and draft regulatory reports without clicking through the Dashboard. Turn full-cycle verification into an AI-powered workflow that moves at the speed of conversation.

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…footprint, heights, site plan, section, written notice and elevations. Pieces that need real-world data (location map, landscape insertion, photos) are listed as to be supplied, never invented. - Plan the construction schedule trade by trade, with dates computed from the quantities. - Issue a drawi… …s: checks, schedules and estimates are indicative technical aids — not an official certification, a regulatory approval or a substitute for an architect, an engineer or a building inspector. Local zoning (PLU) is not checked. Building rules are mainly French. Outdoor works (driveway, networks, lands…

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…m specializing in the global foreign exchange (Forex) industry. It aggregates and verifies official data from over 60 regulatory authorities worldwide. The platform features a scoring system that evaluates brokers across five key dimensions: Regulation, License, Risk Control, Software, and Business. The final results…

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…results and a source sheet. Limits: up to 100 LEIs, 25 company names or 10 parent lookups per call. Data is the GLEIF golden copy at the publication date shown, published three times a day; a change at an issuing unit may appear in the next publication. Name search uses registered legal names; tradi… …shown as its ELF code. Generated files expire in about an hour. This is a data check, not legal or regulatory advice.