What is ISO/TS 23303 about?
Chinese materia medica products manufacturing process is a complicated control system engineering including equipment, technology and quality. The manufacturing process proposed in ISO/TS 23303 is a part of traditional Chinese materia medica control system engineering.
ISO/TS 23303 specifies the whole manufacturing process of Chinese materia medica products by defining a set of domain constraints of sanctioned characteristics, each composed of a relationship and an applicable categorial structure. It includes three process categories: processing, extracting and preparation.
ISO/TS 23303 describes types of manufacturing process, systematic terminology definitions and semantic links between adjuvant materials and processing, extracting, and preparation, which helps in production management and metadata analysis.
NOTE: ISO/TS 23303 is not applicable to Japanese traditional KAMPO medicinal products.
Who is ISO/TS 23303 for?
ISO/TS 23303 on categorial structure for Chinese materia medica products manufacturing process is useful for:
- Healthcare industries
- Healthcare professionals (pharmacists, physicians)
- Academic organizations in the field of pharmaceutical healthcare
- Research and development companies
- Production management of Chinese medicine
Why should you use ISO/TS 23303?
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.
ISO/TS 23303 provides a categorial structure for the manufacturing process of Chinese materia medica products, which helps to improve the scientific level of production management of Chinese medicines and you can classify a wide variety of dosage forms and manufacturing process accurately.