Originally created by biomedicinal subject matter experts, Emtree is Elsevier’s authoritative life science thesaurus. It includes over 90,000 entities covering a wide range of topics, including drugs and medical devices, diseases and biological functions and medical procedures, as well as broader society and the environment.
Emtree is used to index the full text of journal articles in Embase – Elsevier’s comprehensive biomedical and pharmacological literature database – in a consistent and uniform manner. This enables researchers to stay ahead of the ever-accelerating pace of research and development, whether that is conducting systematic literature reviews, monitoring drug safety, or complying with medical device regulations.
SciBite helps by further enriching and optimizing the Emtree thesaurus using a combination of our proprietary tools and manual curation, with rules and additional vocabularies. The result is our Emtree VOCab pack, which includes over 2.5 million synonyms. In the following example, the SciBite curated version of the term ‘Hepa filter’ has 72 synonyms compared to the original 17 in Emtree, a selection of which are shown below.
Significantly, SciBite curation ensures relevance when context when applying meaning to unstructured text. For example, medical device names tend to include common words (e.g., Advance, ATOMS, Oxford, Exponent, Absolute). Curators address this problem using a variety of techniques, including making terms case sensitive, including sub-synonyms so that they are only matched if another synonym for the same concept is present in the text, and defining ‘booster’ words to identify the most relevant mentions, such as the type of device or associated surgical procedure.
Until now, the use of Emtree has been confined to indexing the articles within Embase. The creation of the Emtree VOCab expands existing use cases and introduces a host of exciting opportunities, from aligning your data to this common standard, expanding context-aware search results, and powering inferenced-based discoveries and predictive analysis.
With the new Emtree VOCab and TERMite, SciBite’s entity extraction engine, for the first time, users are able to annotate any text-based dataset to align with the Emtree standard. This allows you to search multiple data sources using a common interface such as SciBite Search – SciBite’s next-generation scientific search and analytics platform which offers powerful interrogation and analysis capabilities across both structured and unstructured public data and proprietary sources.
Medical devices are key in patient healthcare, assisting in the diagnosis, prediction, and monitoring of disease, as well as treating and alleviating symptoms. In recent years, governments have sought greater assurances from medical device manufacturers around the quality, safety, and reliability before and after the marketing of these products.
In 2021, the European Union (EU) introduced the more stringent EU 2017/745 regulation  requiring manufacturers to consult with EU-level experts before placing high-risk medical devices into the market. This directive also specifies tighter controls around clinical evaluations, and agencies that certify medical devices. The onus is placed on improving the availability of information about medical devices to patients, and enhancements have been made to the continued vigilance and market surveillance of devices post-marketing.
In May 2022, this regulation was supported by directive (EU) 2017/746, specifically for in vitro diagnostic medical devices such as pregnancy and COVID-19 tests. In February 2021, the UK government passed into law the Medicines and Medical Devices Act 2021  with a similar focus on patient safety.
Emtree has long since been regarded as a gold standard by regulatory agencies, including the European Medicines Agency (EMA) and Food and Drug Administration (FDA). With terminologies including the Medical Device Trade And General Names and Global Medical Device Nomenclature (GMDN), the Emtree VOCab supports those involved in the manufacture and conformity of medical devices, carrying out effectiveness studies, regulatory submissions or the (semi)automated vigilance-monitoring of these products.
Having a detailed, clear, and unambiguous understanding of the methodology used in a given piece of research is key to validating, reproducing, and aligning to best practices in research and development. The ‘procedures’ component of the Emtree vocabulary includes an extensive collection of scientific, medical, and statistical techniques organized by subject. Users are able to couple this vocabulary with SciBite’s extensive biomedical dictionaries, such as Drug, Indication, and HGNC gene, to analyze literature across R&D, clinical, and manufacturing settings to address a wide range of use cases and questions, such as:<
The Emtree Procedures vocabulary, along with Drug, Indication, and HGNC gene, can be used to analyse literature across R&D, clinical, and manufacturing settings for a host of use cases.
The delivery of drugs, medical devices, and medical services is supported by the Emtree ‘health care’ vocabulary. Users are able to select concepts related to health care from multiple dictionaries, including disease management, quality, and economics terms. These may be particularly useful in ELN or admin systems for clean data capture, or economic evaluation of particular diseases or drugs, e.g., what is the “cost of illness” for heart disease or particular drug treatment?
A much broader ‘society and environment’ branch also features in Emtree, providing users with even more options such as finding articles for example pollutants and energy resources or to look for safety information (danger, risk, safety, and related phenomena branches).
For more information about SciBite’s VOCabs and SciBite products, contact us here.
 EUR-Lex, Access to European Union Law, Consolidated text: Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance)Text with EEA relevance https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02017R0745-20170505
 Medicines and Medical Devices Act 2021 https://bills.parliament.uk/bills/2700
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