claude

pharma-ci

Nine skills for pharma and biotech intelligence teams: build a decision-linked watchlist, write importance rules, set up registry, regulatory, launch-signal, market-access and congress monitors, route alerts to an owned review queue, and publish a weekly brief.

0 on GitHubby edoc33v0.1.2MITupdated 1 month agoresearch
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Plugin pharma-ci from marketplace pharma-ci in edoc33/pharma-ci-skills. Commands read from the repo's manifest — 1 month ago.

What it installs

Skills (9)

  • pharma-ci-access-watch

    Build and run a market-access watchlist: payer policy bulletins and formularies, HTA decision pages (NICE, G-BA/IQWiG, CDA-AMC, HAS, ICER) and clinical guideline pages such as NCCN, organised by asset, geography or indication with a named reviewer per row. Use when an access, coverage or guideline q

  • pharma-ci-congress-watch

    Watch congress abstract and program portals (ASCO, ESMO, ASH, AACR and the user's own) on a seasonal cadence, triage each alert by paper type, trial type, patient count, focus and competitor named, and hand medical affairs a coverage queue with an owner and next action per abstract. Use when plannin

  • pharma-ci-launch-signals

    Build a watchlist for competitor launch and commercial questions: brand/HCP and provider pages, pipeline pages, careers, leadership, newsrooms, investor materials and filing lists. Use when a launch-timing or launch-readiness question needs an owned, defensible record of public signals.

  • pharma-ci-registry-watch

    Watch competitor trial records on ClinicalTrials.gov and EU CTIS: one monitor per pivotal record plus one saved-search monitor per sponsor or indication, each with an alert rule, a named owner and a recheck-by date. Use when a CI, regulatory or medical-affairs team needs a defensible record of regis

  • pharma-ci-regulatory-watch

    Watch FDA, EMA, NICE and one national agency: approvals lists, Drugs@FDA records, Orange Book pages, the advisory committee calendar, warning letters, EPAR pages, CHMP highlights and terminated appraisals, each with a rule that leaves housekeeping edits unflagged. Use when a regulatory-intelligence

  • pharma-ci-review-route

    Turn a source alert into someone's work: a review item with source fact, detection time versus publication time, owner, backup, status and next action, and a Microsoft 365 route (shared mailbox, Power Automate, SharePoint list, Teams optional) or a webhook route into the same list. Use when the firs

  • pharma-ci-rule-writer

    Turn a watch question such as "tell me when a competitor's trial slips" into an importance rule that follows the plugin's rule grammar: named fields, thresholds, explicit ignores, counts asked back, one page type, bracketed variables. Outputs the rule as text and as the JSON summalyzer object, with

  • pharma-ci-watchlist

    Turn a therapeutic area, a competitor list, or a launch into a decision-linked watchlist across the five pharma intelligence jobs with known-record and discovery coverage. Produces a two-column Bulk Import CSV, a prompt guide with one rule, owner and recheck date per row, and an optional dry-run cre

  • pharma-ci-weekly-brief

    Turn a week of monitor changes into a one-page brief in which every item connects to a named decision, a named stakeholder and a timeframe. Pulls the workspace feed or per-job changes through the API helper, or accepts pasted alert emails. Use at the end of each review week, or when a stakeholder as

View source on GitHub

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