Abstract
Whether the
pharmaceutical factory has already performed in-plant drug entity
identification, whether the newly-developed drug product has implemented drug
entity identification, the government aspect of company cooperation with the
Department of Health to subsidize pharmaceutical factories to implement drug
entity identification, the government aspect of the Department of Health
arranging project grants to encourage the pharmaceutical factories to implement
drug entity identification, the government aspect of the government’s need to
mandate regulations for drug entity identification, the government aspect of
the government’s need to continue to provide subsidies to pharmaceutical
factories to implement drug entity identification, the implementation aspect of
drugs should implement entity identification, the implementation aspect of
company belief that the implementation of drug entity identification is most
needed by the public, the implementation aspect of company belief that the
implementation of drug entity identification is most needed by medical
institutions, the benefit aspect of company belief that the implementation of
drug entity identification is most beneficial to medical institutions, and the cost aspect of company belief that the
implementation of drug entity identification will increase the manufacturing
costs of the pharmaceutical factories, have a significant impact on the
willingness to cooperate. The site of the pharmaceutical factory had a
significant impact on drug identification implementation, as shown by the
Chi-square test. In addition, the proportion of domestic sales of
pharmaceutical plants and the number of Western drug items had a significant
impact on the ratio of drug entity identification, as found by the chi-square
test.
JEL classification numbers: C83, M15, O31
Keywords: Standardization, Innovation, Drug Entity Identification, Public Health