Addressing the consequences of the corporatization of reproductive medicine.

Med Law Rev

Faculty of Medicine and Health, Sydney School of Public Health, Sydney Health Ethics, The University of Sydney, Sydney, Australia.

Published: November 2024

AI Article Synopsis

  • In Australia and the UK, the rise of commercial and corporate models in assisted reproduction has created a marketplace that enhances patient choice, though this commercialization may compromise care quality.
  • Current regulations focus mainly on the relationships between doctors and patients, or clinics and consumers, neglecting conflicts of interest between clinic-corporations, shareholders, and their duties to patients.
  • The authors propose new regulatory frameworks that better define the responsibilities of both corporations and clinicians to patients and society, and suggest approaches suitable for both Australia's multi-jurisdictional system and the UK’s single jurisdiction.

Article Abstract

In Australia and the UK, commercialization and corporatization of assisted reproductive technologies have created a marketplace of clinics, products, and services. While this has arguably increased choice for patients, 'choice', shaped by commercial imperatives may not mean better-quality care. At present, regulation of clinics (including clinic-corporations) and clinicians focuses on the doctor-patient dyad and the clinic-consumer dyad. Scant attention has been paid to the conflicts between the clinic-corporation's duty to its shareholders and investors, the medical profession's duty to the corporations within which they practice, and the obligations of both clinicians and corporations to patients and to health systems. Frameworks of regulation based in corporate governance and business ethics, such as stakeholder models and 'corporate social responsibility', have well-recognized limits and may not translate well into healthcare settings. This means that existing governance frameworks may not meet the needs of patients or health systems. We argue for the development of novel regulatory approaches that more explicitly characterize the obligations that both corporations and clinicians in corporate environments have to patients and to society, and that promote fulfilment of these obligations. We consider mechanisms for application in the multi-jurisdictional setting of Australia, and the single jurisdictional settings of the UK.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586528PMC
http://dx.doi.org/10.1093/medlaw/fwae018DOI Listing

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