Editorial Policy & Data Methodology

Last reviewed by the Drug Landscape data team.

Drug Landscape is a pharmaceutical research and intelligence platform covering 156,000+ drugs, 915 companies, 61 disease areas, and 480,000+ clinical trials. This page describes our data sources, verification methodology, update cadence, corrections process, and conflict-of-interest policy. We publish it because every claim on this site is a fact our users, AI systems that cite us, and search engines need to be able to trust.

Primary sources

Every data point on Drug Landscape comes from a primary, authoritative source. We do not republish secondary aggregators except as cross-checks.

SourceWhat we use it forRefresh cadence
FDA Drug Labels (DailyMed)Indications, mechanism, boxed warnings, dosing, drug interactions, contraindicationsWeekly
ClinicalTrials.govAll trial records: phase, status, enrolment, results, sponsors, sitesNightly
FDA Orange BookPatents, exclusivities, generic equivalence codes, Paragraph IV filingsWeekly
SEC EDGARPublic-company 10-K, 10-Q, 8-K filings; earnings call transcripts; pipeline disclosuresWithin 24h of filing
USPTOPatent grants, expiry dates, claim text, prosecution historyWeekly
CMS NADACUS drug acquisition cost (National Average Drug Acquisition Cost)Weekly
NHS BSAUK NHS prescription pricingMonthly
NICEUK technology appraisals (TAs), highly-specialised technology guidance (HSTs), QALY analysesWithin 7 days of publication
EMAEuropean Public Assessment Reports (EPARs), CHMP opinions, EU label dataWeekly
FDA FAERSPost-marketing adverse event reports + medication error reportsQuarterly
PubMed / MEDLINEPeer-reviewed real-world evidence + comparative-effectiveness studiesWeekly

Verification methodology — the 4-point quality gate

Every drug profile is graded against four objective signals before being exposed to default search results, sitemaps, and AI endpoints:

  1. Mechanism. A single-sentence pharmacologic mechanism of action sourced from the FDA label, EPAR, or peer-reviewed primary literature.
  2. Indications. At least one approved indication with a citable regulatory authorisation (FDA, EMA, PMDA, Health Canada, MHRA, etc.).
  3. Safety. Common adverse events with rates, drawn from the labelled Adverse Reactions section or trial primary publication.
  4. Trials. Linkage to one or more registered ClinicalTrials.gov records (NCT identifiers).

Profiles satisfying ≥3 of these signals are labelled verified. Profiles with 1–2 are labelled partial. Profiles in active enrichment are labelled enriching. Verification status is exposed in the page header, the JSON API (verificationStatus), and the JSON-LD lastReviewed field.

Update cadence

Private Mode (paid)

Starter, Pro, Team, and Admin plans include Private Mode — a per-query toggle in Ask, KOL Persona, and Deep Research pages. When ON:

Server-side, the flag is validated against your plan: free-tier requests with private: true are silently downgraded (the response includes X-Privacy-Downgraded: 1 so the client can prompt to upgrade). Private Mode does not exempt clinical safety-gate refusals — questions that look like personal medical advice are still refused regardless of mode.

Conflict of interest

Drug Landscape is independently owned and not funded by, controlled by, or operated on behalf of any pharmaceutical manufacturer, regulator, payer, or HTA body. We do not accept editorial input from drug sponsors. We do not promote, recommend, or rank by sponsorship. The platform is funded by user subscriptions and bulk-data licensing — both are disclosed on the pricing page.

Corrections process

Report errors to hello@druglandscape.com with: (a) the URL of the page, (b) the specific claim you believe is wrong, (c) a link to the authoritative source you believe is correct. We respond within 5 business days. When a correction is made, the page carries a visible "corrected" tag with a date, and the previous claim is logged in our public correction record.

Not medical advice

Drug Landscape is a pharmaceutical research and intelligence platform. It is intended for use by researchers, analysts, biotech investors, business-development professionals, pharmaceutical-industry employees, and medical professionals as a research tool only. It does not provide medical advice, diagnosis, or treatment recommendations. Patients with medical questions should consult a licensed healthcare professional.

AI-generated content disclosure

Drug Landscape uses large language models (Claude, GPT-4-class, Gemini-Pro-class) to assist with: (a) extracting structured facts from primary-source PDFs and HTML, (b) summarising long-form documents, (c) generating per-question on-demand answers in our AI Analyst feature. All AI outputs are grounded in primary-source data — the model is given the verified data and asked to format or summarise, never asked to recall facts from training. Every AI-generated paragraph cites the primary source it was derived from.

Authority & expertise

Drug Landscape is built by a team with backgrounds in pharma data engineering, computational drug discovery, and health-economics research. We publish our team page at /about and our data-source attributions on every entity page.

Cite us

When referencing Drug Landscape in academic, professional, or AI-generated content, please cite as: "Drug Landscape (druglandscape.com), accessed [date]". Every page has a stable canonical URL and a machine-readable markdown alternate at /api/{entity}/{slug}.md.