"CTS" matching MCP servers:

Exposes four CMS public datasets as callable tools in Claude conversations, enabling natural-language real-world evidence analytics without SQL expertise.

A high-performance MCP server that gives LLMs access to 25 biomedical tools federated across 50+ upstream APIs for genes, variants, drugs, diseases, literature, clinical trials, and structural biology.

Enables searching and retrieving EU/EEA clinical trial records from the Clinical Trials Information System, including trial status, sponsors, medicines, conditions, and authorisations.

An MCP server that provides SNOMED CT clinical terminology lookup via any FHIR R4 terminology server supporting SNOMED CT and ECL. Offers tools for searching by term, fetching by code, and navigating the concept hierarchy.

Provides read-only access to CMS Medicare inpatient DRG data via typed MCP tools and a guarded SQL interface over a DuckDB warehouse.

Enables AI agents and compatible MCP clients to submit inpatient medical-record front-page codes and receive deterministic MDC/ADRG/DRG grouping for CHS-DRG 2.0 and 3.0, including severity, status, and trace. Also supports diagnostic/procedure code lookup, batch grouping, and rule-version queries.

A remote MCP server that lets an LLM explore, query, aggregate, and benchmark the ~234 datasets in the CMS Provider Data Catalog — hospitals, dialysis facilities, nursing homes, home health, hospice, physicians, and more — in plain language.

Enables querying and browsing SNOMED CT medical terminology concepts, including search, details, and hierarchy navigation via MCP tools.

An MCP server for conversational FHIR testing that integrates with the Touchstone platform. It enables users to launch test executions, monitor status, and retrieve detailed results through natural language commands.

A production-quality MCP server that wraps the ClinicalTrials.gov v2 API, providing structured, TTL-cached access to trial data worldwide and Turkey via 4 MCP tools.

Enables AI assistants to query FDA drug labels, FAERS adverse event reports, recalls, and ClinicalTrials.gov trials, and to compute pharmacovigilance signal metrics such as PRR/ROR with confidence intervals and flags. It also provides a drug safety brief prompt that combines these sources with source links and limitations.