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Books on the topic 'Access to Essential Medicines and Health Technologies'

Author: Grafiati

Published: 5 June 2025

Last updated: 16 July 2025

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1

Embrey, Martha A. MDS-3: Managing access to medicines and health technologies. 3rd ed. Edited by Management Sciences for Health (Firm). Kumarian Press, 2013.

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2

Pedro, Roffe, Tansey Geoff, and Vivas Eugui David, eds. Negotiating health: Intellectual property and access to medicines. Earthscan, 2005.

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3

Anyama, Nobert. The role of the Health Facility Management Committee in improving community health and access to essential medicines: A case study of Kachonga Sub County, Tororo District. NURRU Publications, 2004.

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4

Suerie, Moon, ed. Informal norms in global governance: Human rights, intellectual property rules and access to medicines. Ashgate, 2012.

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5

Hassoun, Nicole. Global Health Impact: Extending Access to Essential Medicines. Oxford University Press, Incorporated, 2020.

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6

Incentives For Global Public Health Patent Law And Access To Essential Medicines. Cambridge University Press, 2010.

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7

Rubenstein, Kim, Thomas Pogge, and Matthew Rimmer. Incentives for Global Public Health: Patent Law and Access to Essential Medicines. Cambridge University Press, 2010.

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8

Rubenstein, Kim, Thomas Pogge, and Matthew Rimmer. Incentives for Global Public Health: Patent Law and Access to Essential Medicines. Cambridge University Press, 2010.

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9

Rubenstein, Kim, Thomas Pogge, and Matthew Rimmer. Incentives for Global Public Health: Patent Law and Access to Essential Medicines. Cambridge University Press, 2010.

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10

Rubenstein, Kim, Thomas Pogge, and Matthew Rimmer. Incentives for Global Public Health: Patent Law and Access to Essential Medicines. Cambridge University Press, 2010.

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11

Rubenstein, Kim, Thomas Pogge, and Matthew Rimmer. Incentives for Global Public Health: Patent Law and Access to Essential Medicines. Cambridge University Press, 2014.

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12

(Editor), Pedro Roffe, Geoff Tansey (Editor), and David Vivas-Eugui (Editor), eds. Negotiating Health: Intellectual Property and Access to Medicines. Earthscan Publications Ltd., 2006.

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13

(Editor), Pedro Roffe, Geoff Tansey (Editor), and David Vivas-Eugui (Editor), eds. Negotiating Health: Intellectual Property and Access to Medicines. Earthscan Publications Ltd., 2006.

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14

Regional Strategy for Improving Access to Essential Medicines in the Western Pacific Region 2005-2010. World Health Organization, 2005.

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15

De Lima, Liliana, Lukas Radbruch, and Eduardo Bruera. Essential medicines for palliative care. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0003.

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The essential medicines concept developed by the World Health Organization (WHO), states that there is a list of minimum medicines for a basic health-care system, including the most efficacious, safe, and cost-effective ones for priority conditions. According to the WHO, essential medicines are those that satisfy the primary health-care needs of the population. Thus, they should always be available, affordable, and cost-effective. However, the vast majority of the global population does not have access to essential medicines. Many organizations have called on governments to adopt policies to improve availability of these essential medicines and developed programmes and projects to increase awareness and knowledge. This chapter describes two such projects developed by the International Association for Hospice and Palliative Care (IAHPC), based on the essential medicines concept to improve access to medicines and appropriate palliative care: the IAHPC List of Essential Medicines in Palliative Care and the Opioid Essential Prescription Package.

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16

Wizemann, Theresa M., Bruce M. Altevogt, Sheena M. Posey, Diane E. Pankevich, and Forum on Neuroscience and Nervous System Disorders. Improving Access to Essential Medicines for Mental, Neurological, and Substance Use Disorders in Sub-Saharan Africa: Workshop Summary. National Academies Press, 2014.

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17

Medicine, Institute of, Board on Global Health, Board on Health Sciences Policy, Bruce M. Altevogt, and Forum on Neuroscience and Nervous System Disorders. Improving Access to Essential Medicines for Mental, Neurological, and Substance Use Disorders in Sub-Saharan Africa: Workshop Summary. National Academies Press, 2014.

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18

Medicine, Institute of, Board on Global Health, Board on Health Sciences Policy, Bruce M. Altevogt, and Forum on Neuroscience and Nervous System Disorders. Improving Access to Essential Medicines for Mental, Neurological, and Substance Use Disorders in Sub-Saharan Africa: Workshop Summary. National Academies Press, 2014.

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19

Improving Access to Essential Medicines for Mental, Neurological, and Substance Use Disorders in Sub-Saharan Africa: Workshop Summary. National Academies Press, 2014.

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20

Hassoun, Nicole. Global Health Impact. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780197514993.001.0001.

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Every year 9 million people are diagnosed with tuberculosis, every day more than 13,400 people are infected with AIDs, every 30 seconds malaria kills a child. Many people suffer and die young because they cannot access essential medicines. This book argues that people have a right to access these medicines and proposes some new Global Health Impact labeling, investment, and licensing strategies that encourage pharmaceutical companies to improve global health (global-health-impact.org/new). The idea is to rate these companies based on their medicines’ impacts. Highly rated companies will get a Global Health Impact label to use on their products. Socially responsible investment companies and universities might also take the ratings into account in making investment or licensing decisions. After arguing that people do have a right to access essential medicines, this book explores this proposal, its philosophical justification, and its prospects for success.

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21

Krishnaswamy, Sudhir, and Divij Joshi. THE PHILOSOPHY AND LAW OF INFORMATION REGULATION IN INDIA. Centre for Law and Policy Research, 2022. http://dx.doi.org/10.54999/2c0l1p0r.

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India is immersed in several simultaneous battles over the regulation and control of information. While the COVID-19 pandemic has ignited concerns over state-mandated information gathering of the health and personal information of residents, the expanded use of the Aadhaar biometric identity system threatens to make it an essential cipher for every interaction between the state and citizens. At the same time, the earlier momentum towards building strong legislative mandates to disclose public information to promote government accountability and enhance service delivery appears to have stalled. Further, the legislative efforts to regulate both public and private use of personal and non-personal information proceeds at a glacial pace. While these developments occur in different containers and niches of the legal ecosystem, they are grounded in one common conceptual, philosophical and legal puzzle: how should we regulate the access to, and the use of, information by public and private actors? This question becomes all the more salient with the surge in new forms of information collection and processing at a speed and scale made possible by big data collection and algorithmic decision-making technologies. ‘The Philosophy and Law of Information Regulation in India’ project is an effort to collate inter-disciplinary scholarship on the subject of the law and philosophy of information regulation, with a specific focus on India. We recognise that such an effort cannot be bound by legal scholarship alone, and must encompass and contend with the normative assumptions of various approaches towards information technologies.

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22

Schindel, David E., Diane C. DiEuliis, and Bruce Geyman. The Unique Role of Federal Scientific Collections: Infrastructure Generating Benefits, Serving Diverse Agency Missions. Smithsonian Institution Scholarly Press, 2023. http://dx.doi.org/10.5479/si.24559996.

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<p dir="ltr">Scientific research and development are essential in the government, private, and academic sectors of American society. Scientific collections, both living and non-living, are critical components of the U.S. government’s R&D infrastructure, essential for ensuring national security, protecting the public’s health and safe food supply, promoting innovation and economic growth, and protecting the environment. To pursue their diverse long-term missions, U.S. departments and agencies have created and preserve scientific collections to address new and unpredictable challenges to society and to establish long-term baseline histories for the analysis of change, often using new analytical technologies. Federal scientific collections serve the public good by providing access to objects of scientific value regardless of where, when, by whom, or for what reasons they were originally collected and preserved. </p><p dir="ltr">The White House National Science and Technology Council’s Interagency Working Group on Scientific Collections (IWGSC) has, since 2005, convened representatives from 24 Federal departments and agencies that rely on scientific collections. IWGSC has produced a series of studies, reports, and other information resources aimed at improving policies, transparency, accessibility, management, and the assessment of costs and benefits related to Federal scientific collections. This report summarizes these achievements and the IWGSC's future directions, and presents 21 case studies showing how Federal scientific collections have served the nation in diverse areas of American life. </p>

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