SciTransfer
Organization

MINISTERU GHAS-SAHHA U L-ANZJANITA ATTIVA

Malta's health ministry contributing national health data, rare disease governance, and public health policy expertise to European research consortia.

Public authorityhealthMTThin data (2/5)
H2020 projects
3
As coordinator
1
Total EC funding
€370K
Unique partners
180
What they do

Their core work

Malta's Ministry for Health and Active Ageing is the national government body responsible for health policy, public health infrastructure, and healthcare regulation in Malta. Within H2020, it has contributed to European health research coordination — hosting the 2017 EU eHealth Conference during Malta's Council Presidency, participating in rare disease research networks, and supporting COVID-19 population health data infrastructure. Its role is that of a policy authority bringing national health system data and regulatory perspective to EU research consortia.

Core expertise

What they specialise in

Public health policy and data infrastructureprimary
2 projects

PHIRI focused on population health research infrastructure and COVID-19 data, while EJP RD involved health data sharing and FAIR principles.

Rare disease governance and patient empowermentsecondary
1 project

EJP RD addresses rare diseases through shared data access, patient training, and public-private partnerships.

eHealth and digital health policysecondary
1 project

EHW17 was the High Level eHealth Conference organized during Malta's EU Council Presidency in 2017.

COVID-19 population health monitoringemerging
1 project

PHIRI specifically targeted COVID-19 population health research using metadata standards and international comparisons.

Evolution & trajectory

How they've shifted over time

Early focus
eHealth policy coordination
Recent focus
Health data and rare diseases

The Ministry's H2020 involvement began with a high-profile policy event — the 2017 EU eHealth Conference during Malta's Council Presidency — reflecting a focus on digital health diplomacy. From 2019 onward, the focus shifted decisively toward health data infrastructure, rare disease research networks, and pandemic response. The recent keyword set (FAIR data, omics, patient empowerment, COVID-19) signals a move from policy convening toward active participation in data-driven health research.

Moving from one-off policy events toward sustained engagement in European health data sharing and disease-specific research networks.

Collaboration profile

How they like to work

Role: third_party_expertReach: European36 countries collaborated

With 180 unique partners across 36 countries from just 3 projects, the Ministry operates exclusively within very large consortia — typical for CSA and EJP funding schemes. It has coordinated once (EHW17) but more commonly joins as a participant or third party, contributing national health system perspective rather than leading research. This is a policy-level partner, not a research lab — expect institutional authority and national data access rather than hands-on technical work.

Despite only 3 projects, the Ministry has an unusually broad network of 180 partners in 36 countries, driven by participation in large European Joint Programmes and coordination actions. This gives them wide exposure across European health research institutions and national health authorities.

Why partner with them

What sets them apart

As Malta's health ministry, they bring something most research partners cannot: direct authority over a national health system plus access to population-level health data for a well-defined island population. Malta's small size makes it attractive for pilot studies and health data projects where complete national coverage is feasible. For consortium builders, they offer a guaranteed pathway to policy uptake — results don't just sit in reports, they can influence national health policy directly.

Notable projects

Highlights from their portfolio

  • EHW17
    Coordinated the EU High Level eHealth Conference during Malta's 2017 Council Presidency — the largest funded project at EUR 300,000 and the Ministry's only coordinator role.
  • EJP RD
    The European Joint Programme on Rare Diseases is one of the flagship health programmes in H2020, running until 2024, connecting the Ministry to a massive rare disease research network.
  • PHIRI
    Directly addressed COVID-19 population health data needs, demonstrating the Ministry's role as a national data provider for pandemic response research.
Cross-sector capabilities
Digital health and eHealth systemsPublic health data governanceHealth policy and regulatory frameworksPopulation-level data for social science research
Analysis note: Only 3 projects with limited funding data (one project shows no EC contribution as third party). The profile reflects a government ministry with policy-level involvement rather than deep research capacity. The broad partner network (180 partners, 36 countries) is inherited from participation in very large consortia rather than indicating active bilateral collaborations. Analysis should be treated as indicative rather than definitive.