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Learning from Cancer Drug Fund (CDF) in England: A special reimbursement pathway for high-cost cancer drugs

The Cancer Drug Fund (CDF) is a dedicated source of funding in England for increasing patient access to high-cost cancer drugs, with a fixed budget of £340 million per year, operating since 2016. The CDF follows the appraisal by the National Institute of Health and Care Excellence (NICE) whic

Experience in Using HTA for Expanding UHC Benefit Package to Cover Rare Diseases and High-Cost Drugs among Seven Middle and High-Income Countries: A targeted literature review

This policy brief provides a summary of a recent review of the definition of rare diseases, high cost and how HTA has been used in the case of rare diseases in seven countries. The countries were purposively selected based on them having established HTA policies and availability of resources in the

Rare diseases – Talk of the Town for Some Time but What’s Next?

Because of their rarity, rare diseases are often treated with what the industry refers to as ‘orphan drugs’. These group of drugs are quite expensive because of the fewer number of people suffering from such sickness and usually provide low profit to manufacturer compared to other common drug for n

South Korea’s Experience of Reimbursing High-Cost Medicines

Cost-effectiveness and availability of alternative treatment options play a crucial role in the listing of new medicines in South Korea. However, high-cost medicines with no alternative treatment options, particularly those for treating cancer and rare diseases, were not reimbursed under the traditi

Implementation of a Virtual Consultation Platform (VCP) for Healthcare Providers Integrated with a Patient-Facing Mobile Application

– NUHS telemedicine service was developed to improve patients’ and caregivers’ convenience in accessing patient care and to prepare for future crises that hinder in-person clinical consultation  – The key enablers of the telemedicine service were mainly due to strong cross-collaboration between t

eSanjeevani, the National Telemedicine service: Bridging healthcare gaps in India

– eSanjeevani was developed primarily to tackle the challenges of inequitable healthcare access and the shortage of healthcare professionals in India  – The ‘one application’ approach ensured that only one application is used for the national telemedicine service delivery, thus ensuring interoper

Strategies for Sustainable Access: Unpacking Managed Entry Agreements (MEAs) and Innovative Medicine Access

MEAs aim at early access to high-cost innovative medicines at pre-determined terms that can ensure the financial sustainability of healthcare systems. However, their successful adoption hinges on a consideration of various factors to address the unique challenges faced by different nations. The a

Unveiling Thailand’s Path to Open Data for Health Policy

Open data is widely recognized as valuable, especially during the COVID-19 pandemic, highlighting the need for up-to-date information systems, leading all sectors to acknowledge its significance in enhancing efficiency, fairness, and societal development. These open data movements observed during

Cost-Effectiveness of Cascade Testing for Familial Hypercholesterolemia in Thailand: A Comparative Analysis of Genome Sequencing Methods Across Development Stages

Familial Hypercholesterolemia (FH) is a genetic disorder characterized by elevated cholesterol levels, significantly increasing the risk of heart disease. Early detection through genetic screening can play a crucial role in preventing serious health outcomes. This study marks the first global eco

How Does the Health System Impact Our World?: Health, Economic, and Environmental Impacts of IntravenousVersus Oral Paracetamol for Surgeries

– The pharmaceutical industry is a significant emitter of carbon emissions, which accelerates climate change and directly affects human health and health systems. – The safety and efficacy profiles of intravenous (IV) and oral paracetamol for patients undergoing surgeries are comparable. – Swi
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