Data for Health Initiative

Background

Approximately half of all deaths in the world go unrecorded without a cause. This means many health policy decisions are based on inadequate — or often, inaccurate — information. The Data for Health Initiative, launched by Bloomberg Philanthropies in 2015, helps low- and middle-income countries improve the quality of data on births, deaths and noncommunicable disease (NCD) risk factors. The goal: equip governments with the information needed to design better-informed public health policies and save lives. Partnering in over 25 countries, the initiative emphasizes country-led programs and collaborations with governments and global organizations.

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Civil Registration and Vital Statistics 

Strengthening civil registration and vital statistics (CRVS) systems is a critical focus of the Data for Health Initiative. Since 2015, this work has supported more than 37.7 million new or improved birth and death records across partner countries. Activities include: 

  • Assessing and modernizing CRVS systems
  • Enhancing cause-of-death reporting
  • Improving registration practices
  • Producing high-quality vital statistics reports
  • Using best practices to strengthen data collection across regions and populations  

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Data Impact 

The Data Impact (DI) Program empowers countries to expand the use of data to inform public health decision-making. The program provides technical assistance to improve analysis, interpretation, dissemination and use of public health data. Partnering with ministries of health and national public health institutes, the CDC Foundation supports the following DI Program areas: 

  • Data to Policy (D2P) program: Turning data into actionable policy recommendations
  • Public Health Bulletin support: Disseminating information on emerging diseases, outbreaks and surveillance data
  • Scientific Communications trainings: Guiding participants through the process of developing scientific manuscripts  

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NCD Risk Data and Surveillance 

Noncommunicable diseases (NCDs)—including heart disease, cancer, diabetes and chronic lung diseases—account for over 70% of all deaths worldwide, with the greatest burden in low- and middle-income countries. To better monitor these risks, mobile phone-based surveys are a cost-effective method to collect data via SMS (text message) or interactive voice response. This innovative approach helps inform countries’ health policies and strengthen global understanding of NCD trends. The CDC Foundation strengthens NCD risk data and surveillance in these areas: 

  • Supporting countries in using mobile phone technology to collect NCD data
  • Developing globally standardized survey protocols

  • Evaluating the design and delivery of effective mobile phone surveys

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Financial support was provided by the Bloomberg Data for Health Initiative through the CDC Foundation with a grant from Bloomberg Philanthropies.

Program Description: To assist 25 low- and middle-income countries across Latin America, Asia and Africa in strengthening their public health data systems and data use for critical policy-making decisions.
Funding Partners:
  • Bloomberg Philanthropies
Program Partners:
  • CDC’s Global Health Center
  • CDC's National Center for Health Statistics
  • World Health Organization
  • Johns Hopkins Bloomberg School of Public Health
  • Vital Strategies
  • Global Health Advocacy Incubator
  • United Nations Economic Commission for Africa
  • United Nations Economic and Social Commission for Asia and the Pacific
Program Location:
The CDC Foundation supports Data for Health activities in Bangladesh, Ecuador, India, Morocco, Papua New Guinea, Philippines, Rwanda, Solomon Islands, South Africa, Tanzania, Thailand, Uganda and Zambia
Population Health
Global Health
Data for Health