Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12992-018-0421-2
Title: Expanding global access to essential medicines: Investment priorities for sustainably strengthening medical product regulatory systems
Authors: Roth, L.
Bempong, D.
Babigumira, J.B.
Banoo, S.
Cooke, E.
Jeffreys, D.
Kasonde, L.
Leufkens, H.G.M.
Lim, J.C.W. 
Lumpkin, M.
Mahlangu, G.
Peeling, R.W.
Rees, H.
Ndomondo-Sigonda, M.
Stergachis, A.
Ward, M.
Nwokike, J.
Keywords: Access to essential medicines
Regulatory system strengthening
Substandard and falsified
Issue Date: 2018
Publisher: BioMed Central Ltd.
Citation: Roth, L., Bempong, D., Babigumira, J.B., Banoo, S., Cooke, E., Jeffreys, D., Kasonde, L., Leufkens, H.G.M., Lim, J.C.W., Lumpkin, M., Mahlangu, G., Peeling, R.W., Rees, H., Ndomondo-Sigonda, M., Stergachis, A., Ward, M., Nwokike, J. (2018). Expanding global access to essential medicines: Investment priorities for sustainably strengthening medical product regulatory systems. Globalization and Health 14 (1) : 102. ScholarBank@NUS Repository. https://doi.org/10.1186/s12992-018-0421-2
Rights: Attribution 4.0 International
Abstract: Access to quality-assured medical products improves health and save lives. However, one third of the world's population lacks timely access to quality-assured medicines while estimates indicate that at least 10% of medicine in low- and middle-income countries (LMICs) are substandard or falsified (SF), costing approximately US 31 billion annually. National regulatory authorities are the key government institutions that promote access to quality-assured medicines and combat SF medical products but despite progress, regulatory capacity in LMICs is still insufficient. Continued and increased investment in regulatory system strengthening (RSS) is needed. We have therefore reviewed existing global normative documents and resources and engaged with our networks of global partners and stakeholders to identify three critical challenges being faced by NRAs in LMICs that are limiting access to medical products and impeding detection of and response to SF medicines. The challenges are; implementing value-added regulatory practices that best utilize available resources, a lack of timely access to new, quality medical products, and limited evidence-based data to support post-marketing regulatory actions. To address these challenges, we have identified seven focused strategies; advancing and leveraging convergence and reliance initiatives, institutionalizing sustainability, utilizing risk-based approaches for resource allocation, strengthening registration efficiency and timeliness, strengthening inspection capacity and effectiveness, developing and implementing risk-based post-marketing quality surveillance systems, and strengthening regulatory management of manufacturing variations. These proposed solutions are underpinned by 13 focused recommendations, which we believe, if financed, technically supported and implemented, will lead to stronger health system and as a consequence, positive health outcomes. © 2018 The Author(s).
Source Title: Globalization and Health
URI: https://scholarbank.nus.edu.sg/handle/10635/210861
ISSN: 17448603
DOI: 10.1186/s12992-018-0421-2
Rights: Attribution 4.0 International
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