HL7 Products - Master Grid

The HL7 International Arden Syntax for Medical Logic Modules (MLMs) is an ANSI-approved American National Standard language for encoding medical knowledge and representing and sharing that knowledge among personnel, information syste...

GELLO, part of the HL7 Version 3 Normative Edition, is a standard query and expression language that provides a suitable framework for manipulation of clinical data for decision support in healthcare. The GELLO language can be used to build...

The HL7 Version 3 Clinical Document Architecture (CDA®) is a document markup standard that specifies the structure and semantics of "clinical documents" for the purpose of exchange between healthcare provi...

This implementation guide (IG) (currently a DSTU) describes how HL7 Version 3 Clinical Document Architecture (CDA) Release 2 is used to record information for a Consult Note. The Consult Note may contain both narrative and coded data. For t...

A Decision Support Service takes in patient data as the input and provides back patient-specific assessments and recommendations.  A Decision Support Service facilitates the implementation of clinical decis...

This HL7 EHR Behavioral Health Functional Profile (EHR BH FP) contains the functions and conformance criteria deemed important for behavioral health care providers' clinical records systems. At a minimum, this profile provi...

The EHR Clinical Research Functional Profile (EHR CR FP) provides high-level functional requirements necessary for using electronic health record (EHR) data for regulated clinical research. It a...

The HL7 International EHR System Functional Model (EHR-S FM) outlines important features and functions that should be contained in an EHR system. Through the creation of functional profiles, this model provides a standard descr...

This project developed an implementation guide constraining CDA Release 2. The implementation guide supports electronic submission of HAI data to the National Healthcare Safety Network. CDC provided NHSN developers, vocab...

The Context-Aware Knowledge Retrieval (Infobutton) specifications provide a standard mechanism for clinical information systems to request context-specific clinical knowledge form online resources. This has become a widely adopted appro...

The HL7 Version 3 Tuberculosis Domain Analysis Model (DAM) represents the clinical processes associated with managing pulmonary tuberculosis (TB) from the point at which patients present themselves at treatment sites, through diagn...

The Version 3 Regulated Product Submission (RPS) Implementation Guide provides technical details (conformance criteria) on using the Regulated Product Submission (RPS) standard. The RPS standard provides a common means of exchange of do...

The Implementation Guide for CDA Release 2 – Level 1 and 2 – Care Record Summary (US realm) describes constraints on the CDA Header and Body elements for Care Record Summary docu...

The Personal Healthcare Monitoring Report (PHMR) is a document that carries personal healthcare monitoring information, or patient measurement data taken by consumer medical devices. The primary use case around which the PHMR ...

This two-volume implementation guide (IG) describes constraints on the Clinical Document Architecture Release 2 (CDA R2) header and body elements for Quality Reporting Document Architecture (QRDA) documents. The Institute of Medic...

The scope of the standard is to define the message for exchanging information electronically between Regulators and Industry, and between sets of regulators. The message provides the ability to desc...

This standard is Retired; retained for historical reference at HL7 but withdrawn from ANSI 2022 June. 

The Clinical Statement model is designed to be used within multiple HL7 Version 3 domain models. Clinical State...

The HL7 Version 3 Claims and Reimbursements Messaging Standard, retired in 2022, provides non-US realm support for generic, pharmacy, preferred accommodation, physician, oral health, vision care and hospital claims for eligibility, autho...

The Infrastructure Management section of the HL7 Version 3 Normative Edition focuses on the development and management of specifications that support the routing of messages to their specified dest...

This product provides a set of global representations for data used in the presentation and communication of healthcare information. This standardized set has been approved by the International Standards Organization’s (ISO) Medic...

The HL7/ANSI standards related to the ISO Identification of Medicinal Products (IDMP) have been retired. The “retired” status only applies to the HL7 publication. The ISO IDMP standards are still active and managed by ISO TC 215.<...

The purpose of the ebXML message wrapper is to provide a secure, flexible transport for exchanging HL7 messages and other content, and potentially other message formats, between message handling interfaces or ebXML Message Service Handl...

CMETs (Common Model Element Types) are a work product produced by a particular work group for expressing a common, useful and reusable concept. They are generally "consumed", or used by both the producing and other work group...

Scheduling is both a domain and a process. As a domain, Scheduling requires a generic set of messages and behavior to implement any number of Scheduling scenarios. As a process, Scheduling can offe...

This topic covers the issuing of queries to medication knowledge base applications for such information as medication monographs, regimens and therapies.

The HL7 Version 3 Standard: Medi...

This revision of the initial topic extends the existing messaging for Order and Administration to cover Institutional settings. Since the 1st normative ballot of January 2013, numerous editorial fixes have been applied, some narra...

HL7 Version 3 Shared Messages are a work product produced for expressing common, useful and reusable message types. A Shared Message can be envisioned as a message type that is reusable in interactions in any of the domains within the HL7 stand...

The HL7 Version 3 Domain Analysis Model: Vital Records (VR DAM) describes the workflows and stakeholders for transmitting birth and death data to and from U.S. vital records systems. The VR DAM desc...

The BRIDG Model is the result of a collaborative effort between CDISC, HL7, ISO, the US FDA, and the US NCI to build a Domain Information Model for Biomedical Research. These groups have participated in the BRIDG development and a...

The purpose of this document is to describe the conceptual-level viewpoints associated with the business requirements that relate to the content, structure, and functional behavior of information important to the Access Control area of th...

The HL7 Reference Information Model (RIM) is a critical component of the HL7 V3 family of standards. It is the root of all information models and structures developed as part of the V3 development process.

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This document provides assistance to healthcare institutions, hospital information systems vendors, consultants, and other support groups that are considering systems development and implementation activities in a multi-system envir...

This standard specifies methods of encoding rich data in HL7 V2 messages, to enable a virtual medical record for clinical decision support (vMR-CDS) to be built out of HL7 V2 data.

The PHR-S FM standard will address the functional needs of Personal Health Record system developers and users. PHR information is expected to be sent, received, or exchanged from multiple systems, including: EHR systems, insurer systems, payer...

This implementation guide (IG) specifies a standard for electronic submission of neonatal care records (NCRs) in a Clinical Document Architecture (CDA), Release 2 (R2) format. This facilitates electronic extraction of a subset of the C...

The Patient Administration standard defines the requirements and specifications to support the interoperability among clinical and non-clinical systems regarding patient encounters and administrative registries.

The Version 2.5.1 Implementation Guide; Orders and Observations; Interoperable Laboratory Result Reporting to EHR (US Realm), Release 1 provides guidance on how to apply the Version 2.5.1 standard to the exchange of laboratory resul...

The HL7 Version 3 Structured Product Labeling (SPL) specification is a document markup standard that specifies the structure and semantics of the content of authorized published information that accompanies any medicine licensed by a ...

This product page contains the Release 1 Informative Standard of HL7 Version 2.5.1 Implementation Guide: Electronic Laboratory Reporting to Public Health.   If you are seeking the Release 2 Draft Standard for Trial Use o...

The Healthcare, Community Services and Provider Directory specifies core functionality of a Services and Provider Directory that not only supports semantic interoperability, but also valuable business initiatives such as Wait List Manag...

This HL7 Version 3 implementation guide offers supplemental material for the January, 2004 annotated ECG (aECG), standard. This implementation guide is not complete in itself and should be used in conjunction with the HL7 aECG stand...

Describes the basic requirements needed for using the Stability standard and the requirements needed for submitting information to the Food and Drug Administration (FDA) using the standard. This impl...

Data standards support seamless interchange of electronic information within the healthcare environment. The purpose of the cardiovascular domain analysis model (CV DAM) is to facilitate collection of structured data during the care deliv...

This document describes constraints on the Health Level Seven International (HL7®) Clinical Document Architecture (CDA®) Release 2 - Continuity of Care Documents (CCD) specification to support personal health record data ...

This document provides assistance to healthcare institutions, hospital information systems vendors, consultants, and other support groups that are considering systems development and implementation activities in a multi-system envir...

The content of the Laboratory Test Compendium Framework is a Laboratory’s DOS. The content is owned by the sending laboratory for the purpose of being used by the compendium consumer to be able to order laboratory services and t...

HL7 Version 3 Standard: Clinical Trial Registration and Results (CTR&R), Release 1 represents the behavioral and information requirements for the CTR&R domain.  It serves as a tool for subject matter experts to exami...

This document provides technical conformance criteria for Structured Product Labeling (SPL) files based on the drug establishment registration and drug listing process at the United States Food and ...

A Progress Note documents a patient’s clinical status during a hospitalization or outpatient visit, thus is associated with an encounter. The method used to develop the HL7 Implementation Guide for CDA Release 2: Progress Note,...

This document provides a technical messaging specification for transmitting death related information using the HL7 Version 2.6 ADT Update Patient Information. The reporting requirements are consistent with the 2003 Revision of the Unite...

There are many score systems in use in health care at large (Wikipedia). Many systems are in use on an international, national or just hospital wide or individual practice level. Others are just for scientific purposes. Most interesting score...

The schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part of this specification. While HL7 publishes schem...

The HL7 Version 2 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part ...

The HL7 V2.5 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itsel...

The HL7 Version 2.6 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part ...

Technical corrections to HL7 Version 2.4 Messaging Standard.

This addendum is provided to add clarity to implementations of the HL7 version 2.4 messaging standard which choose to follow guidelines for implementing the standard with an XML encoding.  This addendum does not affect imple...

This addendum is provided to add clarity to implementations of the HL7 version 2.3.1 messaging standard which choose to follow guidelines for implementing the standard with an XML encoding.  This addendum does not affect imple...

v2.xml Example Messages

This is an informative document that proposes privacy and security policy relevant data to be exchanged among application systems via an audit message. It is meant to supplement existing system-specific security audits with healthcare appli...

The CDA Implementation Guide for Care Record Summary, Release 2, Discharge Summary provides disparate hospital systems a standard format to report back to a primary care provider or other parties interested in the patient's hospital care....

Sample HMD files for RIM-Based Application Architecture (java SIG) are an unballoted contribution to complement the HL7 Version 3 product suite, developed in 2002.

This document is a non-balloted HL7 Recommendation that describes how to send HL7 messages using public Internet mail.

Recommendations for HL7 Messaging Over Component Technologies Version 1.0, Rev. 9, January 12, 1998 (doc)  is a specification for a set of rules that enable users to describe  HL7 version 2.2 messages using Autom...

Non-normative test cases provided by Sentillion for HL7 CCOW users.

The HL7 V2.x Message Profiling informative document (2000) provides a guideline for documenting particular uses of HL7 messages. A defined V2.x message profile will be registered with HL7 and may be reused by other HL7 users, movin...

Claims Attachments CDA Header XML Schema and stylesheet files that are provided are not part of the balloted content of the standard. Their use by implementers of the standard is entirely optional. HL7 intends to issue...

The purpose of this document is to describe constraints on the CDA Document Body elements for a Care Record Summary document. A Care Record Summary document contains patient's relevant health history for some time period. It is inten...

The HL7 Blood Bank Donation Services Implementation Guide – U.S. Realm is a messaging specification intended to standardize the electronic transmission of information between system application components in a Blood Bank setti...

SPL release 5 (normative) is an extension of the previous releases of SPL, that all received extensive use in production, especially the releases 1, 3, 4, and 5 (DSTU). In addition to labeling submissions, SPL has been used since 2009 for r...

HL7 Version 3 Standard: Pharmacovigilance - Individual Case Safety Report has two parts: Part 1: The Framework for Adverse Event Reporting, R2 has been published by ANSI as ANSI/HL7 V3 ICSRP1, R2-2...

The Electronic Health Record System Function Model Release 2 builds on Release 1.1 of the model, offering a more comprehensive set of functions and criteria.   The work is informed by industry advances/directions, regul...

A Model Definition Language for Clinical Decision Support (CDS) is a grammar for representing clinical information inputs and outputs that can be used by CDS engines and local clinical information systems. This model defin...

The purpose of the ebXML message wrapper is to provide a secure, flexible transport for exchanging HL7 messages and other content, and potentially other message formats, between message handling interfaces or ebXML Message Service Handl...

The objective of this document is to present alternate encoding rules for HL7 Version 2.3.1 to 2.7 messages (and a mechanism for determining alternate encoding rules for subsequent HL7 2.x versions) based on the Extensible Markup Language XML t...

V2.7.1 provides select updates to Chapters 2B, 2C, 4, and 7 to support the Laboratory Results and Orders Interface implementation guides for Meaningful Use Stage 2 and 3 in the USA.

This guide provides guidance on how to communicate laboratory results in general from a (reference) Laboratory’s LIS to a system interested in lab results, e.g., EHR, Public Health, other Laboratory. It covers general lab resul...

The Health Level Seven Version 3 (V3) Normative Edition—a suite of specifications based on HL7’s Reference Information Model (RIM)—provides a single source that allows implementers of V3 specifications to work with the full ...

This topic provides interactions for exchanging information about medication use for individual patients. The content in this topic includes information about medication use constructed from various sources including: patie...

A QRDA Category III report is an aggregate quality report. Each report contains calculated summary data for one or more measures for a specified population of patients within a particular health system over a specific period of time....

The healthcare system is in the midst of a revolution in healthcare information technology. Central to this revolution are technologies that facilitate health information exchange between providers and promote patient engagement and self-...

The Arden Syntax is a formalism for representing procedural clinical knowledge in order to facilitate the sharing of computerized health knowledge bases among personnel, information systems and institutions. Knowledge bases...

The purpose of this CDA R2 Implementation Guide is to specify a standard for genetic testing reports, targeted at both human readability and machine processability. Genetic tests have recently become an important tool in clinical care that ...

The Care Provision Domain describes information structures and vocabulary used to communicate information pertinent to the care of living subjects, devices, geographic sites, and other physical entities by a responsible care provi...

The Care Provision Domain describes information structures and vocabulary used to communicate information pertinent to the care of living subjects, devices, geographic sites, and other physical entities by a responsible care provi...

This specification has been retired and will be retained for historical purposes.

The intent of the current project is two-fold: carry forward the Implementation Guide for CDA Release 2 CDA Framework for Questionnaire Ass...

ITS R2 uses the ISO datatypes, which were designed in tandem with ITS R2. ITS R2 is required to fully utilize the ISO datatypes. This guide is broken into two parts, the ISO datatypes guide, whic...

The standard is a Domain Information Model (DIM) specific to emergency medical service in the pre-hospital setting.  The DIM is balloted as an informative document to be used as a reference in s...

The objective of this document is to present an Implementable Technology Specification (ITS) for the encoding rules for HL7 Version 3 messages based on the Extensible Markup Language XML.

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The Health Level Seven Version 3 (V3) Normative Edition—a suite of specifications based on HL7’s Reference Information Model (RIM)—provides a single source that allows implementers of V3 specifications to work with the full ...

The Allergy and Intolerance Domain Analysis Model is broad, and is intended to unify a number of international models designed to deal with the documentation and interoperability of allergy and into...

The Patient topic defines messages exchanged with Patient Registries. The Patient information model is not limited to persons; any type of living subject can be registered as a patient. The model includes full information about the l...

This document describes profile constraints on the HL7 V2.5.1 ORU^R01 Unsolicited Observation Message to meet the requirements of the transmission of height and weight data for calculating a patient’s body mass index (BMI)...

The HL7 v3 Nutrition Orders Standard – Universal Realm is a messaging specification intended to standardize the electronic transmission and exchange of nutrition orders including oral diets, enteral nutrition (tube feedi...

The Abstract Transport Specification provides models and mechanism for plug and play interoperability. Within that goal, the HL7 standard defines static and dynamic models for the information exchange that refer to the application layer...

The HL7 Version 2.7.1 XML Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part ...

This document describes constraints on the Clinical Document Architecture Release 2 (CDA R2) header and body elements for the Clinical Oncology Treatment Plan and Summary (COTPS) documents, whic...

Note: ELR Release 2 has been retired. This product page contains the Release 2 Draft Standard for Trial Use of HL7 Version 2.5.1 Implementation Guide: Electronic Laboratory Repor...

This document provides the SAIF artifacts that are relevant for the conceptual modeling, comparable to the Domain Analysis Model according to old methodology. The specification provides the foun...

A Decision Support Service takes in patient data as the input and provides back patient-specific assessments and recommendations.  A Decision Support Service (DSS) facilitates the implementation of clinical decis...

The purpose of a Questionnaire Response document is to capture the health survey answers or answer sets to questions that have been administered to a patient. Questionnaire Response documents enable the capture of responses for surve...

This standard specifies a data model for representing clinical data relevant to clinical decision support.

The vMR is a data model for representing the data that are analyzed and/or produced by CDS engines.  The term vMR has h...

The vMR is a data model for representing the data that are analyzed and/or produced by CDS engines.  The term vMR has historically been used in the CDS community to refer to a simplified repr...

International standard document describing the use of a Healthcare Privacy and Security Classification System (HCS) suitable for automated labeling and segmentation of protected health care info...

The HL7 Security and Privacy Ontology serves to name, define, formally describe, and interrelate key security and privacy concepts within the scope of Healthcare Information Technology, including security policies, privacy polic...

This implementation guide supports the transfer of data elements defined by the American College of Surgeons’ Committee on Trauma for Trauma Registries in a CDA document.

This is the Wire Format Compatible Release 1 Data Types (XML ITS R2B) for datatypes. It implements a subset of the Abstract Data Types R2 with a wire format that is mostly backwards compatible with ITS R1. Note, however, that while the w...

This document seeks to define the common concepts and semantics involved in modeling reasoning within the various aspects of the health quality domain, with the goal of providing a common conceptual foundation that other speci...

The Health Level Seven Version 3 (V3) Normative Edition—a suite of specifications based on HL7’s Reference Information Model (RIM)—provides a single source that allows implementers of V3 specifications to work with the full ...

The HL7 Version 2 Implementation Guide: Clinical Genomics; fully LOINC-Qualified Cytogenetic Model, Release 1 - US Realm details structuring cytogenetics test results into the electronic health record utilizing HL7 version 2.5.1...

Many seemingly healthy babies with Critical Congenital Heart Disease (CCHD) may suffer negative health outcomes if the birth defect is not identified shortly after birth. International efforts have precipitated both program and legis...

Prescribers and pharmacies (pharmacists) for several years have been communicating electronic prescription information using the National Council for Prescription Drug Programs (NCPDP) SCRIPT standard. In July of 2004, sixteen parti...

The Allergy and Intolerance Clinical Models unify a number of international models designed to deal with the documentation and interoperability of allergy and intolerance conditions.  The use ...

The Arden Syntax for Medical Logic Systems Version 2.10 is the latest version of a formalism for clinical knowledge representation that can be used by clinicians, knowledge engineers, administrators and others to implement clinical decis...

The Companion Guide to Consolidated Clinical Document Architecture (CDA) for Meaningful Use Stage 2 provides supplemental guidance to the “HL7 Implementation Guide for CDA Release 2: Integrating Health Enterprise (IHE) Health Story Conso...

The Person topic defines messages exchanged with Person Registries. The Person information model defines common identifying and demographic data elements that might be collected for persons regardless of the roles they play. The model...

Population-based cancer surveillance is critical in North America for cancer control activities aimed at reducing the morbidity and mortality of cancer, the second leading cause of death in the United States (U.S.) and the leading cause...

This standard is an HL7 Clinical Document Architecture (CDA) Implementation Guide for representing data extracted from provider systems as required by the Centers for Disease Control and Prevention's National Center for Health Stati...

The Vital Records birth and fetal death reporting (BFDR) CDA had been first published as an STU in Feb, 2015 and expired in 2017. It provided a format for using HL7's Clinical Document Architecture to transmit medical/health infor...

The Ordering Service is intended to complement existing SOA services and the SAIF Behavioral Framework (BF) for HL7. It will provide a Service Functional Model (SFM) for ordering pharmacy, laboratory, radiology, consult and nutri...

The purpose of this specification is to identify a common model that shall be used to derive and implement metadata information in D-MIMs and Logical Models in a consistent manner for any HL7 specification impacting initi...

This specification is the first release of a Domain Analysis Model for Specimen, documenting the conceptual information requirements for use cases provided by Clinical Genomics, Anatomic Pathology and Public Health Laboratories, as well as th...

This Special Issue of the European Journal for Biomedical Informatics contains selected papers presented at the 15th International HL7 Interoperability Conference (IHIC 2015), 9-11 February 2015 in Prague, Czech Republic.

Population-based cancer surveillance is critical in North America for cancer control activities aimed at reducing the morbidity and mortality of cancer, the second leading cause of death in the United States (U.S.) and the leading cause...

Clinical Quality Language (CQL) is a high-level, domain-specific language focused on clinical quality improvement and targeted at measure and decision support artifact authors and implementers.

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The purpose for this implementation guide is to define how the LOINC Document Ontology can be implemented within systems as a foundation for powerful archiving, data mining, and information exch...

The Health Level Seven Version 3 (V3) Normative Edition—a suite of specifications based on HL7’s Reference Information Model (RIM)—provides a single source that allows implementers of V3 specifications to work with the full ...

The HL7 Version 2.8.1 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part ...

The HL7 Meaningful Use Functional Profile (MU FP) conforms to the HL7 EHR-S FM Release 2.0 and identifies functional requirements and conformance criteria corresponding to US Meaningful Use Stage 1 and 2 certification crite...

The Patient Friendly Language for Consumer User Interfaces IG is sponsored by the Department of Veterans Affairs (VA) and is a result of a focused effort to provide a plain language healthcare vocabulary for patient comprehension. This ...

This two volume guide supports the documentation and communication needs of the expanding Medication Therapy Management (MTM) services arena and the CMS Medicare Part D reporting and patient information requirements for MTM. ...

The Data Access Framework Initiative identifies and recommends standards for the interoperable representation and transmission of data using the notion of a Query Stack which modularizes the various layers of the Data Access Frame...

The purpose of this guide is to ensure that HL7 Version 3 standards, particularly CDA R2, achieve their stated goal of semantic interoperability when used to communicate clinical information that is represented using concepts from ...

The Implementation Guide for CDA (R) Release 2: Data Provenance, Release 1, September 2014 is the result of collaborative efforts between HL7 and the US Health and Human Services Office of National Coordinators Standards and Inter...

A core part of the Patient Administration domain, defines messages for events collectively called ADT (admission, discharge and transfer) or Patient Encounter Management. This project completes definition of the HL7 V3 standard for Patie...

This project developed an implementation guide constraining CDA Release 2. The implementation guide supports electronic submission of HAI data to the National Healthcare Safety Network. CDC provided NHSN developers, vocab...

The Health Level Seven (HL7) Standard applies to the electronic exchange of data in all healthcare environments. Within the context of healthcare messaging, the HL7 standard is primarily concerned with the data content of excha...

The Health Level Seven Version 3 (V3) Normative Edition—a suite of specifications based on HL7’s Reference Information Model (RIM)—provides a single source that allows implementers of V3 specifications to work with the full ...

The PACP document is a CDA document template designed to share information created by an individual to express his or her care and medical treatment goals, preferences, and priorities for some future point in time, under certain circu...

The purpose of this implementation guide (IG) is to specify a standard for electronic submission of electronic initial public health case reports using HL7 Version 3 Clinical Document Architecture (CDA), Release 2 format. This imple...

This implementation guide supports the provision of emergency medical service data from provider agencies to hospital emergency departments using the CDA standard. The clinical specifications were developed by the National EMS Infor...

The Structured Product Labeling (SPL) specification is a document markup standard that specifies the structure and semantics of the content of authorized published information that accompanies any medicine or device licensed by a regul...

This document defines the approval and adoption methodology for non-standards process artifacts; it was developed by Project Services but commissioned by the Technical Steering Committee (TSC).  HL7 has a well-defined metho...

The HL7 Version 2.8.2 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part ...

C-CDA Online: A navigation website for C-CDA 2.1

The Companion Guide to Consolidated Clinical Document Archi...

This project encompasses several years of discussion and work within the HL7 Patient Care Work Group in collaboration with the SOA Work Group and Clinical Decision Support Work Group.  The scope of this specification is to defin...

The Health Level Seven Version 3 (V3) Normative Edition—a suite of specifications based on HL7’s Reference Information Model (RIM)—provides a single source that allows implementers of V3 specifications to work with the full ...

The Clinical Statement model is designed to be used within multiple HL7 Version 3 domain models. Clinical Statement is intended to facilitate the consistent design of communications that convey clinical information to meet specific use c...

FHIRPath is a path based navigation and extraction language, somewhat like XPath. Operations are expressed in terms of the logical content of hierarchical data models, and support traversal, selection and filtering of data. Its desig...

Behavioral Health EHRs must be capable of exchanging substance abuse and mental health information using all the applicable Meaningful Use standard IGs. Implementers need practical guidance on how to instantiate messages and docum...

This implementation guide (Guide) defines the requirements for sending and receiving standards-based electronic attachments. It does so by applying additional constraints onto standards in common use for clinical documentation and by defin...

The Vital Records Domain Analysis Model (VR DAM) is the authoritative statement of foundational requirements for the design and development of health information exchange standards in Health Level Seven (HL7) related to vital...

The HL7 Developmental Screening and Reporting Services Derived Profile, Release 1 identifies the critical EHR capabilities for pediatric Developmental Screening and Reporting services. This standard reference content and funct...

The purpose of this implementation guide (IG) is to specify a standard for a response document for a public health electronic Initial Case Report (HL7 eICR v1.1) using HL7 Version 3 Clinical Document Architecture (CDA), Release 2 forma...

The common product model is used to improve the alignment between the different representations of products used within the body of HL7 Version 3 models. One goal of this effort is to make it possible for there to be a single such ...

The HL7 Meaningful Use 2015 Edition Functional Profile (MU FP) conforms to the HL7 EHR-S FM Release 2.01 and identifies functional requirements and conformance criteria corresponding to US Meaningful Use 2015 Edition EHR I...

The Consumer Mobile Health Application Functional Framework is an HL7 Standard for Trial Use (STU). The primary goals of the Consumer Mobile Health Functional Framework ( cMHAFF ) are to provide a standard against which a mobile app&r...

This document describes constraints on the Clinical Document Architecture Release 2 (CDA R2) header and body elements that are derived from requirements set forth by the Academy of Nutrition and ...

A Decision Support Service takes in patient data as the input and provides back patient-specific assessments and recommendations.  A Decision Support Service facilitates the implementation of clinical decis...

This document describes a value set for use in identifying substances of concern for patients with allergies and intolerances. The list was generated by surveying existing records from large syst...

SMART App Launch 2.1.0 defines a foundational patterns based on OAuth 2.0 for client applications to authorize, authenticate, and integrate with FHIR-based data systems (e.g., Electronic Health Record system, Patient Portal, or Be...

This specification has been retired. Please see: HL7 CDA® R2 IG: C-CDA Templates for Clinical Notes STU Companion Guide, Release 3 - US Realm for UDI related templates.

This document provides data to support submission from providers to the American College of Surgeons’ National Trauma Data Bank

This document is a US Realm implementation guide for immunization messaging. The document covers both submission of vaccination events and patient demographics as well as bi-directional query and response. This document is suitable for u...

C-CDA Online: A navigation website for C-CDA 2.1

The Consolidated CDA (C-CDA) implementation guide contains a library of CDA templates, incorporating and harmonizing previous efforts from Health Level Seven...

This implementation guide (IG) provides consistent guidance for capturing key pregnancy status information in healthcare information technology (HIT) products and contains optional supplemental pregnancy status templates for curre...

The HL7 Version 3 Clinical Document Architecture (CDA®) is a document markup standard that specifies the structure and semantics of "clinical documents" for the purpose of exchange between healthcare provi...

The primary purpose of the Work and Health Functional Profile (WHFP) is to expand the capabilities expressed in the EHR-S FM R2 for managing a patient’s “occupational data for health” (as opposed to occupational data ...

The US Core Implementation Guide (available at http://hl7.org/fhir/us/core/STU5.0.1) is based on FHIR Version R4  and defines the minimum conformance requirements for accessing patient data. The Argonaut pilot implementations, ONC 2015 Editi...

This guide defines optional additions to the C-CDA R2.1 Continuity of Care Document (CCD), Transfer Summary, and Discharge Summary standards. These additional templates are  available for use ...

This Implementation Guide defines secure FHIR export Operations that use this capability to provide an authenticated and authorized client with the ability to register as a backend service and retrieve all data in a FHIR server, data on all p...

Genomics is a rapidly evolving area of healthcare that involves complex data structures. There is significant value in sharing this information in a way that is consistent, computable and that can accommodate ongoing evolu...

This is a vendor-agnostic Health Services Platform (HSP) Marketplace specification for publication, curation, discovery, and distribution of interoperable service implementations. This specification is completely agnostic to progr...

The FHIRcast specification describes the APIs used to synchronize disparate healthcare applications' user interfaces in real time, allowing them to show the same clinical content to a user (or group of users).

The HL7 Version 3 Clinical Document Architecture (CDA®) is a document markup standard that specifies the structure and semantics of "clinical documents" for the purpose of exchange between healthcare provi...

This project defines a FHIR interface to a health insurer's drug formulary information for patients/consumers. A drug formulary is a list of brand-name and generic prescription drugs a health insurer agrees to pay for, at least parti...

The FHIR Implementation Guide (IG) specifies a US Realm FHIR electronic Case Reporting (eCR) implementation guide. It profiles FHIR for electronic initial case report (eICR), Reportability Response and trigger code / business logic...

The HL7 Immunization Functional Profile (of ISO/HL7 10781 Electronic Health Record System Functional Model) describes functional characteristics and conformance criteria supporting immunization management and admin...

Analysis Normal Form (ANF) is a logical model intended to represent a normalized view of aggregate clinical statements for analysis, research, clinical decision support, and other purposes. ANF can be used to represent any clini...

The Arden Syntax for Medical Logic Systems is a structured, executable formalism for the explicit representation of scientific, clinical, administrative, and other knowledge used in clinical decision support systems.  Despite the r...

mCODE™ —short for Minimal Common Oncology Data Elements—is an initiative intended to assemble a core set of structured data elements for oncology electronic health records (EHR...

The Privacy and Security Architecture Framework (PSAF) is the overarching package that contains four balloted specifications and an informative guide.  The specific normative components include: 1) Trust Framework for Feder...

The Basic Provenance Informative guide provides the functional and technical guidance for communicating ‘Minimum Viable Provenance’ in CDA, and FHIR, when information is exchanged.

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HL7 Version 2 Conformance Methodology explains the procedures and processes for constraining HL7 v2 message specifications, encompassing both message profiles and implementation guides that contain message profi...

An International Patient Summary (IPS) document is an electronic health record extract containing essential healthcare information about a subject of care. The IPS dataset is minimal and non-exhaustive; specialty-agnostic and condi...

Clinical Decision Support for Immunizations is increasingly being used in health information systems to indicate which vaccinations a patient is due for next. Many of these expert systems are buil...

FHIR provides an effective standard for sites and sponsors to utilize in exchanging clinical research laboratory data. The end-to-end process includes site data storage, site data preparation/transformation, production of FHIR forma...

This cross-paradigm Implementation Guide (IG) is intended to support implementers and enable EHRs to exchange standards-based messages, documents, and resources with other EHR systems using HL7 Meaningful Use IGs and emerging IGs .

This implementation guide describes a framework method for the communication of relevant notifications to support the real-time exchange of information that impacts patient care and value based or risk based services. Providers and Payers may n...

The document aims to provide a reasonable coverage of intra-procedural anesthesia - its content is intended to represent the content of the conventional anesthesia record and to support its electronic equivalent. It includes behavioral and s...

This implementation guide describes the CARIN for Blue Button® Framework and Common Payer Consumer Data Set (CPCDS), providing a set of resources that payers can display to consumers via a FHIR API.

Prior Authorization Support allows a provider's system to request authorization of products and services using FHIR where the content may be altered downstream to conform to HIPAA or other regulated specifications.

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Provides a mechanism for healthcare providers to discover guidelines, pre-authorization requirements and other expectations from payor organizations related to a proposed medication, procedure or other service assoc...

The Food and Drug Administration is standardizing mental health data elements for Bipolar and General Anxiety disorder for drug authorization submissions. Even though there is some standardization across the industries there are v...

This U.S. implementation guide defines a standardized way for a 'new' payer to access the clinical and financial information held by a previous payer that is necessary to ensure that a member who is switching coverage is able to enjoy...

The Birth Defects Reporting Domain Analysis Model (BDR DAM) is a description of foundational requirements for the design and development of health information exchange standards in Health Level Seven (HL7) related to birth defects repor...

This implementation guide specifies FHIR profiles and other artifacts for the Pharmacist Care Plan, which are derived from requirements set forth by the Pharmacy Health Information Technology (HIT) Collaborative and the National Counc...

The FHIR Clinical Guidelines Implementation Guide (CPG IG) provides a means of creating a computable representation of a narrative clinical guideline that is faithful to guideline intent and supp...

This implementation guide specifies constraints on the Clinical Document Architecture Release 2 (CDA R2) header and body elements for the Pharmacist Care Plan, which are derived from requirements set forth by the Pharmacy Health Infor...

This Implementation Guide (IG) defines the use of FHIR resources to convey measurements and supporting data from communicating Personal Health Devices (PHDs) to receiving systems for electronic medi...

This Service Functional Model API defines Services and API(s) for Consent Management. Consent Management is commonly addressed in regulation in participating jurisdictions. It is informed by the results of the C...

This specification describes the requirements needed to manage terminology produced by a variety of organizations across the healthcare enterprise. The healthcare enterprise needs an extensive terminology foundation and the abili...

This is a FHIR IG that defines birth and fetal death reporting in the USA. Birth and fetal death reporting includes the transmission of data from health care providers to jurisdictional Vital Reco...

This guide is a FHIR Resources Library to support the needs of multiple Vital Records Implementation Guides. It does not provide any use case or scenario specific content or additional guidance on how to use these artifacts, but serves as a ...

This implementation guide provides an HL7 CDA-based set of templates defining the Dental Referral Note and Dental Consultation Note. These standardized documents are intended to support bi-directional information exchange between a medic...

This IG supports electronic submission of line-level medication administration data to the National Healthcare Safety Network (NHSN). The project establishes an electronic submission standard that is vendor-neutral that leverages exist...

This implementation guide provides the FHIR R4 artifacts necessary to construct a Dental Referral Note Bundle and Dental Consultation Note Bundle. These standardized documents are intended to support bi-directional information exchange betwe...

The PACIO Functional Status Implementation Guide (IG) is for exchanging mobility, self-care, and domestic life observations primarily involving post-acute care (PAC) transitions between various heal...

The Common Data Models Harmonization (CDMH) FHIR Implementation Guide (IG) will focus on mapping and translating observational data extracted for Patient Centered Outcome Research (PCOR) and other purposes into FHIR format. The proje...

A foundational implementation guide that defines core profiles, terminologies, methodology and other guidelines that are used by other - and in some cases all Da Vinci implementation guides.

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SMART Web Messaging enables tight UI integration between EHRs and embedded SMART apps via HTML5’s Web Messaging. SMART Web Messaging allows applications to push unsigned orders, note snippets, risk scores, or UI sugge...

HL7 Pediatric Care Health IT Functional Profile is an Informative Standard that describes the electronic health record functionality supporting child health care in the United States. The standard supports the Recommendations for the Volun...

The HL7 Version 2.9 v2.xml Message Definition schema representations are provided for convenience, as the XML schema is a compact and specific way to describe the XML representation. However the schema is not in itself a normative part ...

The Subscription R5 Backport Implementation Guide enables servers running FHIR R4B to implement a subset of R5 Subscriptions in a standardized way.

The goal of publishing this guide is to define a standard metho...

Vital signs are collected on nearly every patient encounter. Oftentimes, the clinician needs to know the patient position, device, body location or method the measures were taken.

Blood pressure as a component of vital signs also...

The Hybrid / Intermediary Exchange FHIR implementation guide provides guidance enabling FHIR REST interactions across one or more intermediaries using a passive approach in which the intermediary is ‘passing through’ the i...