03/08/2024 | Press release | Distributed by Public on 03/08/2024 11:44
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Karen Teber, [email protected]
WASHINGTON (August 3, 2024) - Three high-impact steps could be taken by global health leaders to reshape the global regulatory framework and help address the pressing need for equitable access to diagnostics, therapeutics and vaccines during public health emergencies, say a Georgetown global health law expert and a medical student.
In their "Perspective" published today in the New England Journal of Medicine, Georgetown University School of Health professor Sam Halabi, JD, and George O'Hara, a Georgetown medical student and David E. Rogers Student Fellow, say these reforms aim to enhance the capacity of national regulatory bodies, particularly in low- and middle-income countries, to ensure timely and safe access to essential medical products.
Sam Halabi, JD
The U.S. Food and Drug Administration (FDA) and a select group of national regulatory authorities currently dominate the approval process for medical products. However, this concentration of regulatory capacity in high-income countries has led to bottlenecks and delays in the distribution of critical medical supplies during emergencies, as seen during the COVID-19 pandemic.
A recent analysis highlights that few national regulatory bodies, primarily in high-income countries, meet the World Health Organization's (WHO) stringent criteria for being "highly performing." Approximately three-quarters of WHO member states lack the regulatory maturity to assure their populations of the quality of medical products, including vaccines.
To address these weaknesses, Halabi, who directs the Center for Transformational Health Law at the O'Neill Institute for National and Global Health Law, and O'Hara propose three key measures for the WHO and global health leaders:
"Together, these steps can drive more cohesive responses to future public health emergencies," write Halabi and O'Hara.
The WHO has already initiated steps to reduce reliance on the European Medicines Agency and the FDA by creating a new framework of WHO-listed authorities to replace the stringent regulatory authority designation. However, the authors stress the need for additional efforts to ensure greater national control over vaccine supply and reduce dependence on global entities like COVAX.
"Expansion of regulatory pathways would prioritize public health by enabling diagnostics, therapeutics and vaccines to reach populations sooner," they write. "By taking incremental but high-impact steps based on the WHO's classifications of regulatory systems, global health leaders can mount a more equitable and rapid response."
O'Hara's work was supported by a David E. Rogers Student Fellowship Award.