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Glama

Fda Regulations

by io.github.pipeworx-io

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Idempotent

Create a proactive monitoring subscription to a live-data event stream. Returns the new subscription id. Requires a Pipeworx OAuth account (anonymous + BYO cannot persist subscriptions). Supported types: "sec_8k" (8-K filings matching ticker + item codes — e.g. items:["5.02"] = officer change), "polymarket_edge" (Polymarket↔Kalshi cross-venue mispricings — params:{topic:"fed"}), "fred_series" (new FRED observations — params:{series_id:"UNRATE"}). Delivery channels: feed (always on — pull via recent_alerts or GET registry.pipeworx.io/alerts.json), and optionally email (set delivery:{email:"you@x.com"}) or sms (delivery:{sms:"+15551234567"} — phone must be verified at /account first; 10/day cap).

Input Schema

TableJSON Schema
NameRequiredDescriptionDefault
typeYesSubscription type.
paramsYesType-specific filter. sec_8k: {ticker:"AAPL", items?:["5.02","1.01"]}. polymarket_edge: {topic:"fed", min_spread_bps?:500}. fred_series: {series_id:"UNRATE"}. patent_grant: {applicant:"Apple Inc."}. clinical_trial: {sponsor?:"Pfizer", condition?:"lung cancer", phase?:"PHASE3"} (sponsor or condition required).
deliveryNoOptional delivery channels in addition to the always-on persistent feed. {email:"you@x.com"} sends a templated alert per fired event. {sms:"+15551234567"} sends an SMS per event — must match the verified phone on the caller's account (verify at https://pipeworx.io/account first; 10/day cap). {webhook:"https://..."} POSTs each event JSON to your endpoint, HMAC-signed — the response includes delivery.webhook_secret (whsec_…) ONCE; verify X-Pipeworx-Signature = sha256 HMAC of "<X-Pipeworx-Timestamp>.<raw body>". Auto-disabled after 10 consecutive failing runs.

Schema Changelog

Changes observed during successful MCP inspections. Dates show when Glama detected each change.

  1. First observed

TDQS

A4.2/5.0
Behavior1/5

Does the description disclose side effects, auth requirements, rate limits, or destructive behavior?

The description states 'Create' and 'Returns the new subscription id', implying each call creates a distinct subscription. This contradicts the idempotentHint=true annotation, which suggests idempotent behavior. Thus the description contradicts the annotation.

Agents need to know what a tool does to the world before calling it. Descriptions should go beyond structured annotations to explain consequences.

Conciseness5/5

Is the description appropriately sized, front-loaded, and free of redundancy?

The description is well-structured with clear sections, bullet points, and front-loaded purpose. Every sentence adds value, covering types, delivery, and constraints without unnecessary fluff.

Shorter descriptions cost fewer tokens and are easier for agents to parse. Every sentence should earn its place.

Completeness5/5

Given the tool's complexity, does the description cover enough for an agent to succeed on first attempt?

The description fully covers all relevant aspects: authentication requirements, supported types, parameter details, delivery channels, constraints, and return value. No output schema exists, but the description suffices.

Complex tools with many parameters or behaviors need more documentation. Simple tools need less. This dimension scales expectations accordingly.

Parameters5/5

Does the description clarify parameter syntax, constraints, interactions, or defaults beyond what the schema provides?

Schema coverage is 100%, so baseline is 3, but the description adds significant value by explaining type-specific params, delivery options, phone verification, and caps. It clarifies the meaning and usage of all parameters beyond the schema descriptions.

Input schemas describe structure but not intent. Descriptions should explain non-obvious parameter relationships and valid value ranges.

Purpose5/5

Does the description clearly state what the tool does and how it differs from similar tools?

The description clearly states the verb 'Create' and the resource 'proactive monitoring subscription', and specifies it deals with live-data event streams. It distinguishes from sibling tools like list_subscriptions and unsubscribe by describing the creation act.

Agents choose between tools based on descriptions. A clear purpose with a specific verb and resource helps agents select the right tool.

Usage Guidelines5/5

Does the description explain when to use this tool, when not to, or what alternatives exist?

The description provides explicit when-to-use conditions: requires Pipeworx OAuth account, lists supported types with examples, details delivery channels and their constraints (e.g., phone must be verified, 10 SMS/day cap). It indirectly suggests alternatives for one-time queries.

Agents often have multiple tools that could apply. Explicit usage guidance like "use X instead of Y when Z" prevents misuse.

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TDQS

A3.5/5.0
Disambiguation1/5

The tool set contains near-duplicate query tools (ask_pipeworx, ask_pipeworx_beta, ask_pipeworx_grounded) and many overlapping accessors (deep_research, validate_claim, fda_search, fda_regulation). The server name 'Fda Regulations' is also misleading because the vast majority of tools (e.g., polymarket_*, generate_llms_txt, remember) have nothing to do with FDA regulations, making correct selection extremely difficult.

Naming Consistency2/5

Most names use snake_case, but the verb/noun pattern is inconsistent: some are verb-first (ask_pipeworx, generate_llms_txt, validate_claim), some are noun-first (entity_profile, recent_changes, pipeworx_trending), and the ask_pipeworx_beta/grounded variants break the convention. Some names are also semantically misleading (scan_dependency checks an npm package rather than scanning a dependency).

Tool Count1/5

With 33 tools, this is far too many for a server nominally about FDA regulations; only two tools directly address that domain. Even as a general-purpose data platform, 33 tools is excessive and includes many unrelated utilities (e.g., generate_llms_txt, scan_dependency), making the server's scope unclear and bloated.

Completeness2/5

For the stated FDA regulations purpose, only fda_regulation (get by citation) and fda_search (keyword search) exist, providing basic read coverage but no access to FDA data (drug labels, adverse events, recalls), guidance documents, or regulatory history. The many unrelated tools do not fill these gaps, so the surface is severely incomplete for its apparent purpose.

Resources