Arca FDA, Trials & PubMed
ChatGPT pluginPublic FDA and health records
Arca FDA, Trials & PubMed searches a curated index of public regulatory, clinical, and scientific records and returns results with links to the original source.
What you can search:
- FDA drug records: labels, Drugs@FDA approvals and review documents, complete response letters, warning letters, 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 the evidence behind them.
Limitations: it only searches public records that Arca mirrors, so it has no access to your own documents, patient data, or non-public FDA correspondence. It is read-only and cannot file reports or submissions. Results are research material, not medical advice.
- Featured
- No
not on the featured shelf
Movement
From our daily snapshots over the last 30 days.
Rank by placement
Rank in Scientific research
5 listing changes logged · latest Oct 24: Description, Keywords, Version and 2 more. See what changed
In its category
How this plugin compares with others in the same category. Positions are counted within the category, not across the whole directory.
Scientific research32nd of 34 by placement
| # | Plugin | Position | 7d |
|---|---|---|---|
| 30 | #6414 | 19places up | |
| 31 | #6529 | 41places up | |
| 32 | #6697 | — | |
| 33 | #7850 | — | |
| 34 | #8325 | — |
Example prompts
- “Which patents and exclusivities are listed in the Orange Book for Ozempic?”
- “Find Phase 3 trials of tirzepatide in heart failure.”
- “What does the Ozempic label's boxed warning say?”
- Categories
- Sign-in
- On Install
- Capabilities
- Search FDA drug and device records, Search ClinicalTrials.gov studies, Search PubMed literature, Read the full text of a source record
- Availability
- Available
- Version
- 1.0.2
- Keywords
- 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, package insert, prescribing information, boxed warning, DailyMed, NDC, NDC directory, drug shortages, Orange Book, Purple Book, patents and exclusivity, biosimilars, generic drugs, product-specific guidance, adverse 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, 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 literature, scientific papers, research papers, clinical research, 510k, 510k database, 510k search, NDC lookup, postmarketing requirements, premarket approval, substantial equivalence, post-market surveillance, medicine, medical research, vaccine adverse events, CDC data, citations, clinical evidence, phase 3 trials, drug interactions, labeling
- Created
- October 5, 2026
- More info
- Sponsorship
- Promote this plugin