Scientific Research Codex plugins
Follow your plugin and competitors. Review changes to their positioning, capabilities and published terms, with dated source evidence.
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Scientific Research plugins 2
1–2 of 2All words must match. Use quotes for an exact phrase.
| Plugin / developer | Category | Follow |
|---|---|---|
Cypris QCypris Publisher full description …elligence layer across patents, scientific literature, chemical compounds, companies, and technical markets. Your team can use Cypris Q inside ChatGPT to investigate prior art, freedom to operate, competitive landscapes, technology trends, whitespace opportunities, and other critical questions acros… …ategy, and technical teams that want to make ChatGPT more valuable by extending it with specialized datasets, research workflows, and domain-specific intelligence. Show in context →2 more matching sourcesPublisher description …elligence layer across patents, scientific literature, chemical compounds, companies, and technical markets. Your team can use Cypris Q inside ChatGPT to investigate prior art, freedom to operate, competitive landscapes, technology trends, whitespace opportunities, and other critical questions acros… Show in context → |
Scientific ResearchVersion 1.0.0 | View details → |
Arca FDA, Trials & PubMedArcaSearch Arca's public life-sciences corpus: FDA drug and device records, clinical trials, PubMed literature, VAERS, CDC data, and EU/PMDA ... Publisher keywords · listing 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… …erse events FAERS VAERS MAUDE pharmacovigilance drug safety recalls drug recalls device recalls postmarket requirements 510(k) PMA predicate devices medical devices GUDID UDI AI-enabled devices EU MDR IVDR clinical trials ClinicalTrials.gov PubMed Europe PMC literature search systematic reviews cita… Show in context →2 more matching sourcesPublisher full description …rs, Form 483s, inspections, import refusals, Orange Book, Purple Book, NDC, drug shortages, and postmarket requirements - FDA device records: 510(k), PMA, registrations, GUDID, and MAUDE adverse event reports - ClinicalTrials.gov studies - PubMed and Europe PMC literature, ranked with citation counts and open-access status - VAERS, CDC public-health data, EU expert panels, and BfArM/PMDA device vigilance Who it is for: regulatory affairs, quality, pharmacovigilance, clinical, and medical-affairs teams, and anyone researching drugs, devices, or th… Show in context →Publisher description …c life-sciences corpus: FDA drug and device records, clinical trials, PubMed literature, VAERS, CDC data, and EU/PMDA device vigilance. Show in context → |
Scientific ResearchVersion 1.0.2 | View details → |