Transparency

How we decide what matters

A regulatory monitor is only as good as what it refuses to send you. This page documents the scoring and the gates in full — including the ones we added because our own engine got it wrong. The thresholds below are read directly from the running code, so this page cannot quietly fall out of date.

The path an item takes

  1. 1Poll. 10 government and legislative feeds, daily. Each is named publicly, with the endpoint we read.
  2. 2Diff. Changes are keyed by a content hash, so an amended bill reads as a change and a re-published notice does not read as news.
  3. 3Classify. Each item gets a materiality tier (A/B/C) and a signal score, plus a plain-language summary and a suggested action.
  4. 4Review. Tier A and Tier B are held for a person. Nothing in those tiers reaches the public feed without human approval.
  5. 5Publish. Approved items appear on the feed with a link to the primary source.
  6. 6Deliver. A separate decision from publishing. Most items are never emailed to anyone.

The three materiality tiers

Volume is not thoroughness. Most of what a regulatory sweep catches is real, sourced, and irrelevant to a practice — so we tier it and say which is which, rather than presenting a border-refusal record as though it were a rule change.

Tier A

Critical

default route: Today’s batch

A rule changed, and there is a concrete action a practice must take.

For example: A state enacts a supervision requirement with a January 1 effective date. A GLP-1 comes off the shortage list, ending the compounding basis for it.

Review
Human review, always.
Where it goes
Feed, the weekly Brief, and — only if it clears two more gates below — the daily email.
Tier B

Monitor

default route: Include in Brief

A real regulatory development that does not yet demand an action.

For example: A scope-of-practice bill is introduced and referred to committee. An FDA guidance document opens a comment period.

Review
Human review, always.
Where it goes
Feed and the weekly Brief. Never a standalone email.
Tier C

Background

default route: Feed only

Real, sourced, and on the record — but not something a practice acts on. Mostly single-shipment border actions and routine facility citations.

For example: One shipment of lidocaine refused entry at the border. Nine observations at a manufacturing facility.

Review
Two capped exhaust sources publish automatically (below). Everything else keeps its human.
Where it goes
Feed only. Structurally cannot email.

What has to be true before we email you

All three, always. Any one failing means the item still appears on the feed — it just does not interrupt anyone.

Approving is not sending

These are two separate decisions, and fusing them is what turns a monitor into a nuisance. Approval says “this is true and public”. Delivery says “and here is how it reaches people”. Each approved item is routed explicitly:

Tier A defaults to the daily batch rather than a standalone send, on purpose. Ten critical items on a busy day should be one email, not ten.

The one thing that publishes without a human

Tier-C background exhaust from exactly 2 capped sources — FDA Import Refusal and FDA Inspection Citation — publishes automatically. These are high-volume, low-consequence records that would otherwise bury a human queue. Every other item in every other tier and source waits for a person.

An auto-published item still has to clear every one of these, and anything that fails simply stays in the queue for a human:

Tier C cannot email by construction — the automated publisher does not call the notifier at all. So the worst case for this path is an extra background record on the feed.

Severity labels

The badge on each item is a display of the signal score: CRITICAL at 90 or above, CAUTION at 7089, MONITOR below that. These cuts were raised deliberately: at the original threshold, 63% of the corpus read CRITICAL, which makes the word mean nothing.

What we will not do

See the pipeline’s current state on data status, or the feeds themselves on data sources.