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Documentation Index

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FieldValue
DeveloperCommure (d/b/a Athelas)
ProductAir
Product Version1
CHPL ID[TO BE ASSIGNED]
Certification Date[DATE]
Last Updated[DATE]

Mandatory Disclosure Statement

In accordance with the ONC Health IT Certification Program’s Transparency and Disclosure Conditions and Maintenance of Certification requirements (45 CFR § 170.523(k)(1)), Commure (d/b/a Athelas) provides the following mandatory disclosures regarding the costs, fees, and limitations associated with the certified capabilities of Air.

Relied Upon Software

The following third-party software is relied upon to demonstrate compliance with the associated certification criteria:
ONC CriterionThird-Party Software
§170.315(a)(14) Implantable Device ListNLM AccessGUDID API
§170.315(b)(1) Transition of CareEMR Direct
§170.315(d)(3) Audit ReportsGoogle Spreadsheet

Costs and Fees Disclosure

CapabilityDescription of CapabilityCosts or Fees
§170.315(a)(5) DemographicsEnables users to record, change, and access patient demographic information including race, ethnicity, preferred language, sex, sexual orientation, gender identity, date of birth, and related fields per USCDI v3.Included in standard subscription.
§170.315(a)(12) Family Health HistoryEnables users to record, change, and access a patient’s family health history using SNOMED CT® coded data.Included in standard subscription.
§170.315(a)(14) Implantable Device ListEnables users to record, change, and access UDI information for a patient’s implantable devices, with parsing of UDI data via the NLM AccessGUDID API.Included in standard subscription.
§170.315(b)(1) Transition of CareEnables users to create and receive transition of care / referral summaries formatted as C-CDA R2.1 documents containing USCDI v3 data, with Direct Project secure transport.Included in standard subscription. Optional third-party HISP / Direct fees billed by that provider.
§170.315(b)(2) Clinical Information Reconciliation and IncorporationEnables users to reconcile and incorporate medications, medication allergies, problems, and other USCDI v3 data from a received C-CDA into the patient record.Included in standard subscription.
§170.315(b)(10) Electronic Health Information ExportEnables users to perform a patient-level and population-level export of electronic health information in a computable format, with documented export format published publicly.Included in standard subscription.
§170.315(b)(11) Decision Support InterventionsEnables users to configure and use evidence-based decision support interventions, including drug-drug and drug-allergy contraindication checks, with source attribute management.Included in standard subscription.
§170.315(d)(1) Authentication, Access Control, and AuthorizationVerifies user identity and enforces role-based access controls before granting access to electronic health information.Included in standard subscription.
§170.315(d)(2) Auditable Events and Tamper-ResistanceRecords auditable events (including access, modification, and deletion of ePHI) in a tamper-resistant audit log.Included in standard subscription.
§170.315(d)(3) Audit Report(s)Enables authorized users to generate audit reports based on the recorded audit log data.Included in standard subscription.
§170.315(d)(4) AmendmentsEnables users to amend patient records and append patient-supplied amendment requests.Included in standard subscription.
§170.315(d)(5) Automatic Access Time-OutAutomatically terminates user sessions after a configurable period of inactivity.Included in standard subscription.
§170.315(d)(6) Emergency AccessPermits identified users emergency access to electronic health information.Included in standard subscription.
§170.315(d)(7) End-User Device EncryptionPrevents local storage of electronic health information on end-user devices, ensuring ePHI remains protected.Included in standard subscription.
§170.315(d)(8) IntegrityVerifies the integrity of electronic health information using SHA-256 hashing per §170.210(c)(2).Included in standard subscription.
§170.315(d)(9) Trusted ConnectionEstablishes trusted connections for the exchange of electronic health information using transport-level encryption.Included in standard subscription.
§170.315(d)(12) Encrypt Authentication CredentialsEncrypts stored authentication credentials in accordance with §170.210(a)(2).Included in standard subscription.
§170.315(d)(13) Multi-Factor AuthenticationSupports multi-factor authentication of user identity using industry-recognized standards.Included in standard subscription.
§170.315(e)(1) View, Download, and Transmit to 3rd PartyEnables patients (and authorized representatives) to view, download, and transmit their health information to a 3rd party, including a method for requesting restrictions on USCDI v3 data.Included in standard subscription.
§170.315(e)(3) Patient Health Information CaptureEnables users to identify, record, and reference patient-generated health information or data from a non-clinical setting.Included in standard subscription.
§170.315(g)(3) Safety-Enhanced DesignProduct is designed using a user-centered design process (NISTIR 7741) with usability testing across required certification criteria.Included in standard subscription.
§170.315(g)(5) Accessibility-Centered DesignProduct development incorporates accessibility-centered design standards across applicable certified capabilities.Included in standard subscription.
§170.315(g)(6) Consolidated CDA Creation PerformanceProduct creates C-CDA documents conforming to C-CDA R2.1 Companion Guide Release 4.1 from source data and does not act as a pass-through.Included in standard subscription.
§170.315(g)(7) Application Access — Patient SelectionProvides a documented API for application access to patient selection.Included in subscription. No registration, sandbox, or production fees. §170.404(a)(4) fair-and-reasonable fees may apply for value-added services.
§170.315(g)(9) Application Access — All Data RequestProvides a documented API for application access to all data for a single patient, returning USCDI v3 data formatted per C-CDA R2.1.Included in subscription. No registration, sandbox, or production fees. §170.404(a)(4) fair-and-reasonable fees may apply for value-added services.
§170.315(g)(10) Standardized API for Patient and Population ServicesProvides a FHIR R4 API conforming to US Core IG v6.1.0 and SMART App Launch v2.0.0 for patient and population-level data access by third-party applications.Included in subscription. No per-app, per-call, volume, registration, sandbox, or production fees. §170.404(a)(4) fair-and-reasonable fees may apply for value-added services.

Limitations and Types of Costs Affecting Implementation, Use, or Interoperability

  • Additional software required: No additional third-party software is required for customers to implement or use the certified capabilities of Air, beyond the relied upon software listed above which is included as part of the product.
  • Contractual limitations: None. There are no contractual limitations that restrict a customer’s use, transfer, modification, or exchange of data using the certified capabilities of Air.
  • Technical limitations: None. There are no technical limitations affecting interoperability or data portability of the certified capabilities of Air.
  • Limitations on customer modifications: None. There are no limitations on customer-initiated modifications to the certified capabilities of Air.

Contact

For questions about this disclosure, please contact Commure (d/b/a Athelas) support at support@athelas.com.