QD-MCP

ClaudeCommunityby Pharm·ology

QD [Quantify Decisions] by Pharm·ology turns public clinical and regulatory data into decision-ready drug development intelligence inside your AI assistant. Ask in plain language or call commands directly to: • Build disease landscapes for a condition, mechanism, or therapy area — pipeline, approvals, recruitment benchmarks, efficacy & safety, and regulatory interactions — as a branded page or Excel workbook. • Map the competitive field (mechanism × stage × company) and visualize pipelines. • Benchmark trial operations: recruitment/accrual medians (ClinicalTrials.gov and EU CTIS, reported separately), design parameters, sites, and eligibility. • Pull FDA + EMA approvals and disciplinary-review findings, an FDA interactions dossier with verbatim meeting Q&A, and regulatory read-across. • Retrieve per-endpoint efficacy, adverse events by relative risk, and PubMed references. Every quantitative result is traceable to its public source — the major international clinical-trial registries and regulatory agencies, including ClinicalTrials.gov, EU CTIS, the FDA, EMA, MHRA and Health Canada, among others, plus PubMed — with records hyperlinked to the original and coverage expanding over time. QD is read-only. Requires a QD subscription. Request access at [email protected].