Access detailed information on test procedures, guidelines, indications, and more, all in one convenient platform.

Source: Mayo, ARUP, & LabCorp

Access a centralized database that stores and organizes imaging requirements for various diseases. This includes specifications for recommended imaging modalities such as MRI, PET, CT, X-ray, Ultrasound, and more.

Source: Mayo, ARUP, & LabCorp

Access comprehensive information on rare and ultra rare diseases; signs, symptoms, diagnosis, treatment guidelines, and other inquiries.

Source: Mayo, ARUP, & LabCorp

Ask any question about biomarkers, genes, mutations, and other molecular data relevant to various diseases.

Source: Mayo, ARUP, & LabCorp

Use lookup mode to search for specific variants, genes, or rsIDs. Use conversation mode to delve deeper into selected details.

Source: LitVar, a platform developed by the National Center for Biotechnology Information (NCBI)

Efficiently cross-reference medical and billing codes such as ICD-9 and ICD-10, along with corresponding information from numerous vocabularies.

Source: Athena OHDSI Vocabularies Repositories (20+)

Access and compare recent regulatory guidelines and approvals segmented by region.

Source: FDA, EMA, TGA, ICH

Summarize the drugs and doses used in a anti-neoplastic regimen used in treating all cancers and other diseases.

Source: ARUP, Mayo, LabCorp

Provide recent response assessment criteria for all cancers. The copilot provides details into how we classify responses as complete, partial, stable, progressive, or other categories as appropriate per disease.

Source: ARUP, Mayo, LabCorp

Quickly create and review protocol-specific ICFs that comply with regulatory requirements and with institution-specific template and format. Leverage our templates or upgrade to customize the template to suit your needs.

Accelerate the writing process of your proposals, manuscripts, and other documents by real time researching biomedical data sources and quickly synthesizing that research into a summary for you.

Simplify the feasibility questionnaire creation and responses, streamlining communication between Sites, Sponsors, and CROs, while reducing manual work and accelerating appropriate site selection.