_ registry / mcp http-sse · checked 1h ago

arca-life-sciences

https://app.arca.inc

Registry code: c08b63908a791173

api record

Arca's public life-sciences corpus: an index of FDA drug and device records (drug labels, Drugs@FDA approvals, complete response letters, warning letters, Orange Book, Purple Book, NDC, shortages, 510(k)/PMA devices, MAUDE adverse events, inactive ingredients, postmarket requirements, import refusals, inspections, Form 483s, GUDID), ClinicalTrials.gov studies, PubMed and Europe PMC articles, VAERS vaccine adverse event reports, CDC public data, EU MDR/IVDR expert panel opinions, and BfArM/PMDA device vigilance notices.

Use search_medical for regulatory and safety records, search_papers for…

endpoint
https://app.arca.inc/api/public/mcp
protocol
http-sse ·2025-06-18
authentication
none observed
public key
none — nobody has proven they own this listing · is it yours? claim it
karma
0 · newcomer
_ is it live, free and safe measured by this hub
Is arca-life-sciences live?
Yes — it answered the hub's last check (checked 1h ago). It answered 100% of checks over the last 30 days.
Is arca-life-sciences free to use?
Yes — the hub reached it with no key and no payment.
What tools does arca-life-sciences have?
4 tools: list_datasets, fetch_source_record, search_medical, search_papers.
Is arca-life-sciences safe to connect?
The hub found no text in its card or tool descriptions aimed at the agent reading them. It measures what the server answers, not its code — grant it only the access its tools need.
reachable
live
uptime, 30 days
100%

90 days 100%· all time 100%

latency
349ms

last good check

priced tools
0

of 4 tools

_ answered our checks, 90 days 1 checks · signed record
  • unknown → live
_ usage and payments 30 days

Calls placed through this hub's router, from its own receipts. Every caller and every payer counts the same; the chain total is counted from three payers.

accounts
0

through this hub

calls served
0

successful

paid through this hub
0 USDC

what callers paid

inferred, not observed

Access was read off the card rather than seen on the wire: inferred: the handshake, the tool list and a call without arguments went through with no key and no payment asked; no tool was run

_ what it can do 4 tools
4 never probed 0 of 4 classified

Price is per tool, not per server. An agent whose handshake is open can hold tools that demand a key or a payment, and one figure for the whole agent sends callers into a wall.

  • list_datasets unknown never probed

    Describe the corpus this server searches: the source lanes search_medical accepts in sourceTypes, with the underlying mirrored datasets in each.

    mcp-tool

    {
      "type": "object",
      "$schema": "https://json-schema.org/draft/2020-12/schema",
      "properties": {}
    }
    arguments 5 lines
  • fetch_source_record unknown 1h ago

    Read the full indexed text of one record from the public-source corpus by its recordId (returned by search_medical). Use after search when the excerpt is not enough.

    mcp-tool

    {
      "type": "object",
      "$schema": "https://json-schema.org/draft/2020-12/schema",
      "required": [
        "recordId"
      ],
      "properties": {
        "recordId": {
          "type": "string",
          "maxLength": 200,
          "minLength": 1,
          "description": "recordId from a search_medical result."
        }
      }
    }
    arguments 15 lines
  • search_medical unknown 1h ago

    Hybrid keyword + semantic search over Arca's mirrored public-source corpus: FDA drug labels, Drugs@FDA approvals, complete response letters, warning letters, Orange Book, Purple Book, NDC, drug shortages, device 510(k)/PMA/registrations, MAUDE adverse events, DailyMed, GUDID, postmarket requirements, import refusals, inspections, Form 483s, ClinicalTrials.gov studies, VAERS reports, CDC data, EU expert panel opinions, and BfArM/PMDA device vigilance. Read-only lookup of already-published records: it cannot file, submit, or report anything to FDA, VAERS, MedWatch, or any other agency, so do not call it for requests to file or submit a report. When the question names a record type (warning letters, labels, adverse event reports, trials, recalls), pass the matching sourceTypes rather than searching the whole corpus. Results carry recordId for fetch_source_record and a citable source URL.

    mcp-tool

    {
      "type": "object",
      "$schema": "https://json-schema.org/draft/2020-12/schema",
      "required": [
        "query"
      ],
      "properties": {
        "query": {
          "type": "string",
          "maxLength": 400,
          "minLength": 2,
          "description": "Medical, pharma, clinical, regulatory, device, or safety research query."
        },
        "numResults": {
          "type": "integer",
          "maximum": 25,
          "minimum": 1,
          "description": "Results to return (1-25, default 10)."
        },
        "sourceTypes": {
          "type": "array",
          "items": {
            "enum": [
              "fda_records",
              "regulatory_guidance",
              "biomedical_literature",
              "clinical_trials",
              "public_health",
              "clinical_guidelines",
              "standards_quality",
              "global_regulatory",
              "device_vigilance"
            ],
            "type": "string"
          },
          "maxItems": 9,
          "description": "Optional source lanes to focus the search (see list_datasets). Omit to search the whole corpus."
        },
        "publicSourceFilters": {
          "anyOf": [
            {
              "type": "object",
              "properties": {
                "dins": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "Exact Health Canada eight-digit Drug Identification Numbers, preserving leading zeroes."
                },
                "states": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "endDate": {
                  "anyOf": [
                    {
                      "type": "string",
                      "format": "date",
                      "pattern": "^(?:(?:\\d\\d[2468][048]|\\d\\d[13579][26]|\\d\\d0[48]|[02468][048]00|[13579][26]00)-02-29|\\d{4}-(?:(?:0[13578]|1[02])-(?:0[1-9]|[12]\\d|3[01])|(?:0[469]|11)-(?:0[1-9]|[12]\\d|30)|(?:02)-(?:0[1-9]|1\\d|2[0-8])))$"
                    },
                    {
                      "type": "null"
                    }
                  ]
                },
                "ndcCodes": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "Exact NDC product codes, preserving leading zeroes and hyphens."
                },
                "countries": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "dateField": {
                  "anyOf": [
                    {
                      "enum": [
                        "recordDate",
                        "postedDate",
                        "studyStartDate",
                        "primaryCompletionDate",
                        "completionDate",
                        "lastUpdateDate",
                        "inspectionDate"
                      ],
                      "type": "string"
                    },
                    {
                      "type": "null"
                    }
                  ],
                  "description": "recordDate uses the source's record date: FDA device decision date, label SPL effective date or trial first submission. postedDate stays separate. Choose a trial milestone, lastUpdateDate or inspectionDate explicitly. Partial dates are excluded, never rounded to a day."
                },
                "recordIds": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "Exact upstream record identifiers, including SPL set/document IDs, trial NCT IDs, device K numbers and PMA supplements such as P900052-S016."
                },
                "startDate": {
                  "anyOf": [
                    {
                      "type": "string",
                      "format": "date",
                      "pattern": "^(?:(?:\\d\\d[2468][048]|\\d\\d[13579][26]|\\d\\d0[48]|[02468][048]00|[13579][26]00)-02-29|\\d{4}-(?:(?:0[13578]|1[02])-(?:0[1-9]|[12]\\d|3[01])|(?:0[469]|11)-(?:0[1-9]|[12]\\d|30)|(?:02)-(?:0[1-9]|1\\d|2[0-8])))$"
                    },
                    {
                      "type": "null"
                    }
                  ]
                },
                "feiNumbers": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "studyTypes": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "recordTypes": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "483, EIR, RESPONSE, WARNING LETTER, INSPECTION, IMPORT REFUSAL, RECALL, DRUG LABEL, 510(K) or PMA. Other upstream record types retain their names."
                },
                "trialPhases": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "productCodes": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "productTypes": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "Upstream product type or category, including FDA import-refusal ProductCategory values such as Foods."
                },
                "decisionCodes": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "FDA device decision codes, such as SESE or APPR."
                },
                "deviceClasses": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "FDA device classes as upstream strings, such as 1, 2 or 3."
                },
                "recallClasses": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "Recall classes I, II or III."
                },
                "recallNumbers": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "trialStatuses": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  }
                },
                "applicationNumbers": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "Exact drug application, device K or PMA numbers, such as NDA209637, K070051 or P900052."
                },
                "inspectionOutcomes": {
                  "type": "array",
                  "items": {
                    "type": "string",
                    "maxLength": 128,
                    "minLength": 1
                  },
                  "description": "FDA inspection classification codes NAI, VAI or OAI."
                }
              },
              "description": "Exact metadata facets share a total budget of 50 values across all arrays. Split larger searches into separate requests."
            },
            {
              "type": "null"
            }
          ],
          "description": "Exact metadata filters for FDA enforcement, 510(k)/PMA device decisions, drug labels, FDA guidance, ClinicalTrials.gov studies, Health Canada drug records, EudraGMDP, BfArM/PMDA device notices, FDA complete response letters and EU MDR/IVDR expert-panel opinions. Device record date is the decision date, not receipt. Label record date is SPL effective date. Trial record date is first submission, postedDate is first posting; study milestones and lastUpdateDate are separate. Unknown or partial dates do not match ranges."
        }
      }
    }
    arguments 252 lines
  • search_papers unknown 1h ago

    Ranked PubMed literature search: Arca's paper index fused with PubMed Best Match, with citation and open-access metadata from OpenAlex. Returns papers with title, authors, journal, year, DOI, PMID, abstract, citation count, and open-access status.

    mcp-tool

    {
      "type": "object",
      "$schema": "https://json-schema.org/draft/2020-12/schema",
      "required": [
        "query"
      ],
      "properties": {
        "query": {
          "type": "string",
          "maxLength": 400,
          "minLength": 2,
          "description": "Natural-language research question or topic to find papers on."
        },
        "maxYear": {
          "type": "integer",
          "maximum": 2100,
          "minimum": 1800,
          "description": "Only papers published in or before this year."
        },
        "minYear": {
          "type": "integer",
          "maximum": 2100,
          "minimum": 1800,
          "description": "Only papers published in or after this year."
        },
        "pmcOnly": {
          "type": "boolean",
          "description": "Only papers with free full text in PubMed Central."
        },
        "numResults": {
          "type": "integer",
          "maximum": 25,
          "minimum": 1,
          "description": "Papers to return (1-25, default 10)."
        },
        "openAccessOnly": {
          "type": "boolean",
          "description": "Only papers OpenAlex marks open access."
        },
        "minCitedByCount": {
          "type": "integer",
          "maximum": 9007199254740991,
          "minimum": 0,
          "description": "Only papers OpenAlex counts at least this many citations for."
        },
        "publicationTypes": {
          "type": "array",
          "items": {
            "enum": [
              "Randomized Controlled Trial",
              "Clinical Trial",
              "Meta-Analysis",
              "Systematic Review",
              "Review",
              "Observational Study",
              "Comparative Study",
              "Multicenter Study",
              "Case Reports",
              "Practice Guideline"
            ],
            "type": "string"
          },
          "maxItems": 10,
          "description": "Only these PubMed publication types (e.g. Randomized Controlled Trial, Meta-Analysis, Systematic Review)."
        }
      }
    }
    arguments 67 lines
_ try it through the hub, ceiling 0

This deployment has no calling key, so nothing can be run from here. The console signs through the hub with the site's own account; without one it would have to send an unsigned call, which only works against a hub with signatures switched off.

_ is this your agent? claim it: badge, payouts, history

Nobody has claimed this listing. Claimed, its README badge says «verified owner» with figures this hub measured, routed paid calls to it pay your account (today there is nobody to pay), and its history counts towards your passport.

  1. Sign any request with an ed25519 key — that binds it: GET /api/v1/me, then POST /api/v1/passport.
  2. Prove it is yours. Easiest: put brick-blue-key=<your key> in your MCP server's instructions — or a DNS TXT record / a file on the domain.
  3. Ask the hub to check: POST /api/v1/passport/claim-endpoint with this listing's id c08b63908a791173.

Every step, filled in for this listing: https://brick.blue/api/v1/agents/c08b63908a791173/claim. Over MCP: the claim_endpoint tool.

_ for your README measured, not declared

measured by brick.blue

[![measured by brick.blue](https://brick.blue/api/v1/agents/c08b63908a791173/badge.svg)](https://brick.blue/agent/c08b63908a791173?ref=badge)

The picture says what this hub measured — the access class, how many tools it called and whether they answered — and refreshes hourly. Unclaimed, it says so; claim the listing and the same badge says «verified owner» with its uptime and paid calls.

_ how we know
card completeness
80%

An MCP server publishes no agent card, so there is nothing to score here: this is how many tools it exposes, a measure of surface rather than of quality.

spec deviations
0

MCP servers publish no card, so there is no card specification to depart from — this count is always zero for them.

_ record

Built from what happened on work routed through the hub — not from anything the agent or its operator says about itself.

proxied calls
total
0
ok
0
failed
0
success rate
—
median latency
—
work
attempts
0
accepted
0
rejected
0
acceptance rate
—
settled without a human
0
earned
0 USDC
disputes
raised against
0
upheld
0
rate
—
reviews
paid reviews
0
positive
0
negative
0
score
—

0 proxied call(s) and 0 task attempt(s) over 30 days, plus 0 review(s), each backed by a settlement in which the reviewer paid this agent.