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FAIRsharing.grqm4q; Last edited: Jan. 8, 2019, 1:34 p.m.; Last accessed: Jan 03 2022 7:12 p.m.

Other names: CDISC PRM

Names

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CDISC Protocol Representation Model

metasource: Fairsharing.org
version: FAIRsharing.org: CDISC PRM; CDISC Protocol Representation Model; DOI: https://doi.org/10.25504/FAIRsharing.grqm4q; Last edited: Jan. 8, 2019, 1:34 p.m.; Last accessed: Jan 03 2022 7:12 p.m.

CDISC PRM

The CDISC Protocol Representation Model (PRM) provides a standard for planning and designing a research protocol with focus on study characteristics such as study design, eligibility criteria, and requirements from the ClinicalTrials.gov, World Health Organization (WHO) registries, and EudraCT registries. PRM assists in automating CRF creation and EHR configuration to support clinical research and data sharing.

Description

More detailed information about this field from each metasource.

The CDISC Protocol Representation Model (PRM) provides a standard for planning and designing a research protocol with focus on study characteristics such as study design, eligibility criteria, and requirements from the ClinicalTrials.gov, World Health Organization (WHO) registries, and EudraCT registries. PRM assists in automating CRF creation and EHR configuration to support clinical research and data sharing.

Webpage:

https://www.cdisc.org/standards/foundational/protocol

Webpage

More detailed information about this field from each metasource.

https://www.cdisc.org/standards/foundational/protocol

Tags:

Tags
More detailed information about this field from each metasource.

protocol
metasource: Fairsharing.org
version: FAIRsharing.org: CDISC PRM; CDISC Protocol Representation Model; DOI: https://doi.org/10.25504/FAIRsharing.grqm4q; Last edited: Jan. 8, 2019, 1:34 p.m.; Last accessed: Jan 03 2022 7:12 p.m.

protocol

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CDISC Glossary seeks to harmonize definitions (including acronyms, abbreviations, and initials) used in the various standards initiatives undertaken by CDISC in clinical research. Glossary also serves ...

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BRIDG is a domain analysis model that represents the realm of protocol-driven clinical, pre-clinical, translational and basic research. This breadth includes concepts from Common (i.e., concepts share ...

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An interactive retrieval system for clinical trial studies with context-dependent protocol elements. Clinical trial protocol includes all the steps that should be conducted in clinical trial and all ...

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ClinicalTrials.gov, a largest source of clinical trials data in the US, is a Web-based resource that provides patients, their family members, health care professionals, researchers, and the public wit ...

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WHO Adverse Reaction Terminology

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Some of the resources used by the system:

® FAIRsharing.org
® Bioontology/Bioportal Terms
® Nucleic Acid Research - Database
® re3data.org
® bio.tools
® PubMed - Courtesy of the U.S. National Library of Medicine