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Risk Identification and Regulation for China's Anti-Commercial Bribery in Medical Device Procurement and Sales Industry.

Created on 23 Sep 2025

Authors

Jie Fu, Jing-Yi Xu, Yue Wang

Published in

Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih. Volume 40. Issue 2. Pages 144-149. Jun 30, 2025.

Abstract

In China, the regulatory framework for medical device procurement and sales, particularly concerning anti-commercial bribery, relies heavily on punitive mechanisms applied after violations occur. Consequently, there is an urgent need to establish a scientific risk regulation framework as a complementary approach. Effective risk-oriented regulatory models require precise identification of risk areas in commercial bribery. Focusing on several major procurement scenarios such as centralized bulk-buying, tendering and bidding processes, in-hospital procurement, and online purchasing, this article analyzes the structural factors contributing to these risks, represented by the absence of certification mechanisms, lack of transparency in information disclosure, and inadequate checks and balances. Based on official risk assessment results, this study applies the theory of power and responsibility to propose a preventive regulatory framework that combines industry self-discipline and administrative oversight. By combining these approaches, the framework aims to develop regulatory measures that can effectively reduce commercial bribery risks and prevent illegal and non-compliant conduct.

PMID:
40985063
Bibliographic data and abstract were imported from PubMed on 23 Sep 2025.

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