Information model of Chinese materia medica processing

This document specifies an information model within the field of Chinese materia medica processing. It defines a set of domain constraints of sanctioned characteristics, each composed of a relationship and an applicable information model. This model aims at representing the concepts applicable to Chinese materia medica processing in the making of decoction pieces. This document is not applicable to Japanese traditional Kampo medicine.

Titre manque

General Information

Status
Published
Publication Date
19-Jan-2020
Current Stage
9093 - International Standard confirmed
Start Date
20-Nov-2023
Completion Date
13-Dec-2025
Ref Project

Overview

ISO/TS 21831:2020 - Information model of Chinese materia medica processing is a Technical Specification published by ISO (first edition, 2020) that defines an information model for the processing of Chinese materia medica (CMM) into decoction pieces. Prepared by ISO/TC 215 (Health informatics), the document establishes domain constraints, characterizing categories and semantic links to represent the concepts and relationships needed to describe processing methods, parameters and outcomes used in Traditional Chinese Medicine (TCM). This specification is explicitly not applicable to Japanese Kampo medicine.

Key topics and requirements

  • Information model definition: graphical and textual representations of entities and relationships (data model / conceptual model) for CMM processing.
  • Domain constraints: set of sanctioned characteristics composed of a relationship plus an applicable information model.
  • Characterizing categories: standardized terms and definitions covering CMM concepts such as decoction piece, processing, adjuvant material, moisture content, ash content, nature (four properties/five flavours), preparation methods (steaming, frying, calcining, blanching, cutting, etc.).
  • Semantic links and categorial structure: explicit relationships (examples include “is processed by”, “change”) that connect entities in a concept diagram (see Figure 1 in the specification).
  • Parameters and metrics: conceptual coverage of measurable factors relevant to processing (temperature, duration, proportion of adjuvant material), leaching/decocting rates, purity and texture indicators.
  • Scope and exclusions: applies to the making of decoction pieces; normative references are none and Kampo medicine is excluded.

Practical applications and users

Who benefits:

  • Health informatics professionals building interoperable data models and clinical information systems for TCM.
  • TCM manufacturers and quality control teams standardizing manufacturing records, processing parameters and traceability of decoction pieces.
  • Clinical researchers and systematic reviewers who need consistent process descriptions to interpret heterogeneity across trials and improve meta-analysis quality.
  • Regulators and standards bodies seeking standard terminology and representation to assess processing quality and consumer safety.
  • Data integrators and software developers implementing electronic records, LIMS or ontology-aligned databases for herbal medicine supply chains.

Practical value:

  • Improves consistency of process reporting for CMM.
  • Enables semantic interoperability and clearer comparison of processing effects on quality, toxicity and effectiveness.
  • Supports data synthesis, traceability and compliance in TCM production and research.

Related standards

This TS uses and aligns terminology with other ISO/IEC resources cited in the text, for example:

  • ISO/TS 18876-2, ISO/IEC 19763-12, ISO/TS 17948, ISO 18668-1, ISO/TS 18062, ISO/TS 20282-2 and ISO 472 (as sources for definitions and concepts).

Keywords: ISO/TS 21831:2020, Chinese materia medica, information model, decoction pieces, TCM processing, semantic links, health informatics.

Technical specification
ISO/TS 21831:2020 - Information model of Chinese materia medica processing Released:1/20/2020
English language
11 pages
sale 15% off
Preview
sale 15% off
Preview

Standards Content (Sample)


TECHNICAL ISO/TS
SPECIFICATION 21831
First edition
2020-01
Information model of Chinese materia
medica processing
Reference number
©
ISO 2020
© ISO 2020
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2020 – All rights reserved

Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
3.1 General . 1
3.2 Characterizing categories . 2
4 Categorial structure . 6
4.1 Overview . 6
4.2 Semantic link . 8
Bibliography .10
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/ directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/ patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see www .iso .org/
iso/ foreword .html.
This document was prepared by Technical Committee ISO/TC 215, Health informatics.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/ members .html.
iv © ISO 2020 – All rights reserved

Introduction
Chinese materia medica is widely utilized as a part of complementary and alternative medicine
throughout East Asia and western countries. In order to ensure the quality and therapeutic effect of
Chinese medicines, it is important to use a proper manufacturing process of Chinese materia medica.
There are guidelines for processing Chinese materia medica in the Traditional Chinese Medicine
industry, and clinical trials are already available. A large number of relevant trials have been conducted
to assess the function of decoction pieces of Chinese materia medica. However, the descriptions of
processing in reports tend to be insufficient for the interpretation of heterogeneity among trials, often
causing difficulties for data synthesis in meta-analyses. This arises from two reasons: firstly, because
of the lack of use of an appropriate information model of the processing of Chinese materia medica, and
secondly because semantic associations between concepts of Chinese materia medica processing have
yet to be explicitly identified.
In order to address these problems, this document defines the information model within the field of
Chinese materia medica processing.
TECHNICAL SPECIFICATION ISO/TS 21831:2020(E)
Information model of Chinese materia medica processing
1 Scope
This document specifies an information model within the field of Chinese materia medica processing. It
defines a set of domain constraints of sanctioned characteristics, each composed of a relationship and
an applicable information model.
This model aims at representing the concepts applicable to Chinese materia medica processing in the
making of decoction pieces.
This document is not applicable to Japanese traditional Kampo medicine.
2 Normative references
There are no normative references in this document.
3 Terms and definitions
For the purposes of this document, the following terms and definitions apply.
ISO and IEC maintain terminological databases for use in standardization at the following addresses:
— ISO Online browsing platform: available at https:// www .iso .org/ obp
— IEC Electropedia: available at http:// www .electropedia .org/
3.1 General
3.1.1
concept
internal conception of some thing; general notion or idea of some thing
[SOURCE: ISO/TS 18876-2:2003, 3.1.3]
3.1.2
entity
any concrete or abstract thing of interest
3.1.3
relationship
association between two or more entities (3.1.2) indicating the purpose or type of association
Note 1 to entry: Can also be known as an association when the information model is based upon object classes.
3.1.4
information model
graphical and textual representation of entities (3.1.2) and the relationships (3.1.3) between them
Note 1 to entry: Can also be known as a data model, a conceptual data model, a logical data model, an entity
relationship model, an object class diagram, or a database definition.
[SOURCE: ISO/IEC 19763-12:2015, 4.2.24]
3.2 Characterizing categories
3.2.1
traditional Chinese medicine
TCM
traditional medicine that originated in China, and is characterized by holism and treatment based on
pattern identification/syndrome differentiation
[SOURCE: ISO/TS 17948:2014, 2.2]
3.2.2
Chinese materia medica
CMM
medicinal parts of medicinal plants, animals, and minerals after preliminary processing (3.2.4), which
are used as raw materials in Chinese medicines
Note 1 to entry: This refers to the raw materials used to make decoction pieces.
[SOURCE: ISO 18668-1:2016, 3.2]
Note 2 to entry: Preliminary processing can include washing and drying. Large and bulking items can also be cut
into smaller pieces or shorter lengths.
3.2.3
decoction piece
prescription medicine processed from Chinese materia medica (3.2.2) under the direction of traditional
Chinese medicine (3.2.1) and processing (3.2.4) methods for Chinese medicines, which can be directly
used in clinical practice or the production of prepared medicines
3.2.4
processing
physical or chemical technique of converting Chinese materia medica (3.2.2) into decoction pieces
(3.2.3) based on the theory of pharmacology of traditional Chinese medicine (3.2.1), the nature of Chinese
materia medica (3.2.30), the need for dispensing, preparation (3.2.19) and clinical application
Note 1 to entry: This definition is taken from Reference [24].
3.2.5
toxicity
ability of a substance to produce an adverse effect upon a living organism
[SOURCE: ISO 472:2013, 2.767]
3.2.6
effectiveness
accuracy and completeness with which users achieve specified goals
[SOURCE: ISO/TS 20282-2:2013, 4.7]
3.2.7
adjuvant material
substance added during processing (3.2.4) in order to enhance the therapeutic usefulness of
pharmaceutical herbal medicament treatment
Note 1 to entry: Adjuvant material is different from excipient material. The latter is usually used to produce pills
or tablets, inseparable from tablets, etc. But the solid adjuvant material is discarded after processing.
[SOURCE: ISO/TS 18062:2016, 3.4, modified — Note to entry has been modified.]
2 © ISO 2020 – All rights reserved

3.2.8
channel tropism
meridian tropism
orientation of the medicinal action according to the meridian/channel on which the therapeutic action
is manifested
Note 1 to entry: This definition is taken from Reference [20].
3.2.9
moisture content
amount of water contained in decoction pieces (3.2.3) after processing (3.2.4)
Note 1 to entry: General moisture content of CMM and decoction shall be controlled between 7 % and 13 %.
Note 2 to entry: This definition is taken from Reference [22].
3.2.10
ash content
basic purity (3.2.12) indicator for the quality control of decoction pieces (3.2.3)
Note 1 to entry: Ash is present in the residue weight of decoction pieces left after incineration at high temperature
(500℃ to 600℃).
Note 2 to entry: Ash content including physiological ash and acid incompatibility ash.
EXAMPLE The total ash content of GLYCYRRHIZAE RADIX ET RHIZOMA (Gancao) is not more than 7 %. The
acid incompatibility ash content is not more than 2 %.
Note 3 to entry: This definition is taken from Reference [22].
3.2.11
texture
shape, size, colour, quality of the herb and decoction pieces (3.2.3)
Note 1 to entry: This definition is taken from Reference [23].
3.2.12
purity
quota of the impurities or non-medicinal parts in processed Chinese materia medica (3.2.2)
Note 1 to entry: This definition is taken from Reference [22].
3.2.13
pressure
exertion of force upon a surface
3.2.14
decoction ingredient
chemical components including bioactive or therapeutic agents, and other invalid chemical constituents
in decoction pieces (3.2.3) which stem from botanical medicine (3.2.16), mineral medicine (3.2.17) and
animal medic
...

Questions, Comments and Discussion

Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.

Loading comments...

Frequently Asked Questions

ISO/TS 21831:2020 is a technical specification published by the International Organization for Standardization (ISO). Its full title is "Information model of Chinese materia medica processing". This standard covers: This document specifies an information model within the field of Chinese materia medica processing. It defines a set of domain constraints of sanctioned characteristics, each composed of a relationship and an applicable information model. This model aims at representing the concepts applicable to Chinese materia medica processing in the making of decoction pieces. This document is not applicable to Japanese traditional Kampo medicine.

This document specifies an information model within the field of Chinese materia medica processing. It defines a set of domain constraints of sanctioned characteristics, each composed of a relationship and an applicable information model. This model aims at representing the concepts applicable to Chinese materia medica processing in the making of decoction pieces. This document is not applicable to Japanese traditional Kampo medicine.

ISO/TS 21831:2020 is classified under the following ICS (International Classification for Standards) categories: 11.020.99 - Other standards related to health care in general. The ICS classification helps identify the subject area and facilitates finding related standards.

You can purchase ISO/TS 21831:2020 directly from iTeh Standards. The document is available in PDF format and is delivered instantly after payment. Add the standard to your cart and complete the secure checkout process. iTeh Standards is an authorized distributor of ISO standards.

記事のタイトル:ISO/TS 21831:2020 - 中国の漢方薬の情報モデル 記事の内容:この文書は、中国の漢方薬の処方方法における情報モデルを定めています。それは、許可された特性のドメイン上の制約条件の関係と適用可能な情報モデルで構成されています。このモデルは、漢方薬の処理における概念を「煎じ薬」として表現することを目指しています。ただし、この文書は、日本の伝統的な漢方医薬には適用されません。

기사 제목: ISO/TS 21831:2020 - 중국 한약 가공의 정보 모델 기사 내용: 이 문서는 중국 한약 가공 분야의 정보 모델을 규정합니다. 이 모델은 인가된 특성들의 도메인 제약 조합으로 이루어진 관계와 적용 가능한 정보 모델을 정의합니다. 이 모델은 중국 한약 가공에서 감수액조각 제작과 관련된 개념을 나타내는 것을 목표로 합니다. 이 문서는 일본 전통 칸포 약초 치료에는 적용되지 않습니다.

The article discusses ISO/TS 21831:2020, which is an information model for Chinese materia medica processing. It defines the relationships and characteristics involved in the processing of Chinese herbal medicine. The model specifically focuses on the production of decoction pieces and is not applicable to Japanese traditional Kampo medicine.