Difference between revisions of "Clinical Research Process Content"
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==Summary== | ==Summary== | ||
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Clinical Research Process Content(CRPC) is part of a set of profiles that create interoperability between EHRs and specialized research systems, resulting in EHR-enabled research. CRPC works with Retrieve Process for Execution to define workflow automation across systems such as EHRs and Clinical Research Management Systems. CRPC is a content profile, but of a particular type of content: the formal definition of processes. CRPC defines a set of processes that EHRs can execute in the completion of a clinical trial. | Clinical Research Process Content(CRPC) is part of a set of profiles that create interoperability between EHRs and specialized research systems, resulting in EHR-enabled research. CRPC works with Retrieve Process for Execution to define workflow automation across systems such as EHRs and Clinical Research Management Systems. CRPC is a content profile, but of a particular type of content: the formal definition of processes. CRPC defines a set of processes that EHRs can execute in the completion of a clinical trial. | ||
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| − | + | CRPC provides a framework to define processes for execution in the EHR: | |
| + | * Study Definition Content Module | ||
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==Benefits== | ==Benefits== | ||
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CRPC addresses the need of healthcare sites to execute research processes as defined in the research protocol. In the current manual workflow, the protocol is read by the study coordinator, and steps such as enrollment and scheduling are manually entered into the site's EHR. With workflow automation provided by RPE and CRPC, the protocol can directly dictate the steps of research execution to the EHR. This, in turn, reduces the workload of the study coordinator, and lowers the cost of performing research studies at healthcare sites. | CRPC addresses the need of healthcare sites to execute research processes as defined in the research protocol. In the current manual workflow, the protocol is read by the study coordinator, and steps such as enrollment and scheduling are manually entered into the site's EHR. With workflow automation provided by RPE and CRPC, the protocol can directly dictate the steps of research execution to the EHR. This, in turn, reduces the workload of the study coordinator, and lowers the cost of performing research studies at healthcare sites. | ||
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==Details== | ==Details== | ||
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The RPE profile sets up actors which hold sections of the research protocol as executable instruction sets. The Process State Manager hands off the executable instructions to the Process Activity Executor, which abides in the EHR. CRPC builds on these actors and transactions, and defines the specific processes to be executed. Through the CRPC-defined process interactions of these actors the research protocol can be executed within the EHR. | The RPE profile sets up actors which hold sections of the research protocol as executable instruction sets. The Process State Manager hands off the executable instructions to the Process Activity Executor, which abides in the EHR. CRPC builds on these actors and transactions, and defines the specific processes to be executed. Through the CRPC-defined process interactions of these actors the research protocol can be executed within the EHR. | ||
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==Systems Affected== | ==Systems Affected== | ||
| − | + | * Electronic Health Record | |
| − | + | * Clinical Trial Management System | |
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==Specification== | ==Specification== | ||
| − | + | Profile Status: [[Comments| Trial Implementation]] | |
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| − | + | Documents: | |
| + | * [[http://ihe.net/Technical_Framework/upload/IHE_QRPH_Suppl_CRPC.pdf Clinical Research Process Content (CRPC) ]] | ||
| + | Underlying Standards: | ||
| + | * HL7 Biomedical Research and Regulation | ||
| + | * CDISC Study Design Model | ||
| + | * Retrieve Process for Execution (RPE) | ||
| + | * Clinical Research Document (CRD) | ||
| − | + | ==See Also== | |
| − | :* | + | Documents: |
| − | : | + | * [[http://ihe.net/Technical_Framework/upload/IHE_QRPH_Suppl_RPE.pdf Retrieve Process for Execution (RPE) ]] |
[[Category:Profiles]] | [[Category:Profiles]] | ||
[[Category:QRPH Profile]] | [[Category:QRPH Profile]] | ||
| + | [[Category:DocShare]] | ||
| + | [[Category:CDA]] | ||
Latest revision as of 15:33, 4 November 2019
Clinical Research Process Content specifies content, which is appropriate to help automate the sharing of information among systems during the clinical research process using the transactions from the Retrieve Process for Execution (RPE) profile.
Summary
Clinical Research Process Content(CRPC) is part of a set of profiles that create interoperability between EHRs and specialized research systems, resulting in EHR-enabled research. CRPC works with Retrieve Process for Execution to define workflow automation across systems such as EHRs and Clinical Research Management Systems. CRPC is a content profile, but of a particular type of content: the formal definition of processes. CRPC defines a set of processes that EHRs can execute in the completion of a clinical trial.
CRPC provides a framework to define processes for execution in the EHR:
- Study Definition Content Module
Benefits
CRPC addresses the need of healthcare sites to execute research processes as defined in the research protocol. In the current manual workflow, the protocol is read by the study coordinator, and steps such as enrollment and scheduling are manually entered into the site's EHR. With workflow automation provided by RPE and CRPC, the protocol can directly dictate the steps of research execution to the EHR. This, in turn, reduces the workload of the study coordinator, and lowers the cost of performing research studies at healthcare sites.
Details
The RPE profile sets up actors which hold sections of the research protocol as executable instruction sets. The Process State Manager hands off the executable instructions to the Process Activity Executor, which abides in the EHR. CRPC builds on these actors and transactions, and defines the specific processes to be executed. Through the CRPC-defined process interactions of these actors the research protocol can be executed within the EHR.
Systems Affected
- Electronic Health Record
- Clinical Trial Management System
Specification
Profile Status: Trial Implementation
Documents:
Underlying Standards:
- HL7 Biomedical Research and Regulation
- CDISC Study Design Model
- Retrieve Process for Execution (RPE)
- Clinical Research Document (CRD)
See Also
Documents: