| 英文摘要 |
The data controller, through the collection and processing of data, can gain in-depth insights into user behavior patterns and preferences, especially in the biomedical field where extensive electronic health data collection and processing can assist in understanding disease mechanisms, timing of medication administration, and clinical diagnoses, ultimately achieving the goal of precision medicine. It is evident that the widespread possession of medical information has become a coveted objective for various enterprises. However, in today’s highly competitive business environment, data controllers are often reluctant to provide their data to competitors free of charge. This behavior may stem from reasons such as maintaining a competitive advantage or safeguarding user data security. Nevertheless, regardless of the rationale, the refusal of data controllers to share data has created obstacles to information flow across platforms. Although the United States has Health Insurance Portability and Accountability Act of 1996, HIPAA to protect patients’rights to transmit data across institutions, enabling patients to address information blockade behavior through HIPAA, commercial entities such as pharmaceutical companies and biotech firms remain powerless when facing information blockade behavior. The situation for commercial entities in our country is even more challenging. Not only does our country lack relevant laws specifically targeting information blockade behavior, but under current regulations, commercial entities are unable to access electronic health data. The inability of commercial entities to freely access electronic health data significantly hampers the discovery, research, and production of new medical products, thereby slowing down the overall development of the biomedical field. Therefore,“information blockade behavior,”especially“biomedical information blockade behavior,”is an urgent problem that needs to be addressed in our country. In regulating such“information blocking”behavior, two pathways widely discussed in academia are the“personal data legal framework”and the“competition legal framework”. The General Data Protection Regulation (GDPR) enacted by the European Parliament, specifically Article 22, serves as a representative of the“personal data legal framework”pathway, recognizing the right of data subjects to transfer their data across platforms, also known as data portability, as an extension of their fundamental rights. On the other hand, the 21st Century Cures Act enacted by the US Congress serves as a representative of the“competition legal framework”pathway. From the perspective of preserving market competition, it expressly mandates data controllers to transfer their data to other competitors to maintain equal footing in the market. It is worth noting that the legislative purpose of the U.S. 21st Century Cures Act is to accelerate the discovery, research, and production of new medical products. Therefore, its content focuses more on granting profit-making entities the right to access electronic health data, which aligns with the aim of this article to address biomedical information blockade behavior and promote the overall development of the biomedical industry. This article approaches the issue from a competition law perspective, with the discussion centered on U.S. law supplemented by EU law, to explore whether current competition law can address information blockade behavior. For example, whether possessing a dominant position is a threshold for competition law regulation; if data controllers who do not hold a dominant position engage in information blockade behavior, whether they may not be subject to current competition law regulations; and whether the essential facilities doctrine can serve as an alternative solution. In terms of legal effects, a key focus of this article is whether measures aimed at restoring market competition can truly revert the market to its original state, and whether these measures are suitable for the market in which electronic health data controllers operate. After discussing the three-tiered question of“whether competition law can address information blockade behavior”, this article will use the U.S. 21st Century Cures Act as a reference to analyze the feasibility of special legislation in competition law to promote cross-platform information exchange. It will explore whether the implementation of this act has benefited electronic health data exchange in the United States, reduced information blockade behavior, and facilitated profit-making entities’utilization of electronic health data. The article aims to stimulate discussions across various sectors regarding the competition law approach, gradually easing restrictions on profit-making entities’access to electronic health data and serving as a reference for future legislative efforts in our country. |