SciTransfer
Organization

UNIWERSYTET MEDYCZNY IM KAROLA MARCINKOWSKIEGO W POZNANIU

Polish medical university combining paediatric health research, pharmaceutical drug delivery science, and medical device regulatory expertise across European consortia.

University research grouphealthPL
H2020 projects
7
As coordinator
1
Total EC funding
€2.3M
Unique partners
115
What they do

Their core work

Poznań University of Medical Sciences is a Polish medical university with strong capabilities in paediatric health research, pharmaceutical sciences, and clinical trials. They contribute epidemiological expertise to large European cohort studies on birth defects, neonatal brain injury, and preterm infant outcomes. They also run a significant training programme in biopharmaceutics and drug delivery (ORBIS), and have recently expanded into medical device regulation and peritoneal dialysis research.

Core expertise

What they specialise in

Paediatric and neonatal health researchprimary
4 projects

Core contributor to SHIPS (preterm infant screening), ALBINO (neonatal brain injury treatment), EUROlinkCAT (congenital anomalies cohort), and ENRICHME (elderly care monitoring).

Birth defect epidemiology and registry linkagesecondary
1 project

Contributed to EUROlinkCAT, linking EUROCAT birth defect registries with hospital discharge and prescription data across Europe.

Medical device regulation and safetyemerging
1 project

Participated in MDOT, their largest-funded project (EUR 897K), focused on MDR compliance, biocompatibility testing, and regulatory databases.

Evolution & trajectory

How they've shifted over time

Early focus
Paediatric clinical health research
Recent focus
Pharmaceutical technology and regulation

In the early H2020 period (2015–2017), the university focused on clinical paediatric health — preterm infant screening, neonatal brain injury, and assisted living for elderly patients. From 2018 onward, their profile broadened significantly: they took on coordination of a pharmaceutical sciences training network (ORBIS), entered the medical device regulation space (MDOT), and joined nephrology research (IMPROVE-PD). This shift suggests a deliberate expansion from purely clinical research toward pharmaceutical technology, regulatory science, and translational medicine.

Moving from clinical observation studies toward applied pharmaceutical R&D and medical device regulation — increasingly positioned at the research-to-market translation boundary.

Collaboration profile

How they like to work

Role: active_partnerReach: European25 countries collaborated

Primarily a consortium participant (5 of 7 projects), stepping into coordination once with ORBIS — a training-focused MSCA network. With 115 unique partners across 25 countries, they are well-connected across European health research networks. Their wide partner base and diverse project types suggest they are a flexible, reliable consortium member rather than a project-driving hub.

Extensive European network spanning 115 unique partners in 25 countries, reflecting deep integration into multi-country clinical studies and training programmes. Geographic reach is pan-European with no apparent regional concentration.

Why partner with them

What sets them apart

They combine clinical medical research with pharmaceutical technology expertise — a relatively rare pairing in Polish academia. Their ORBIS coordination demonstrates capacity to lead international training in drug delivery and biopharmaceutics, while their MDOT participation brings practical knowledge of medical device regulation under the new EU MDR. For consortium builders, they offer a Polish partner with both clinical trial infrastructure and pharmaceutical sciences depth.

Notable projects

Highlights from their portfolio

  • ORBIS
    Their only coordinated project — a MSCA training network in biopharmaceutics and drug delivery, signalling institutional commitment to pharmaceutical sciences.
  • MDOT
    Largest single funding (EUR 897K) and an unusual pivot into medical device regulation, blockchain-based safety databases, and MDR compliance.
  • EUROlinkCAT
    Major European birth defect cohort study linking registry data with hospital records across multiple countries — core epidemiological infrastructure work.
Cross-sector capabilities
Medical device regulation and safety testingPharmaceutical manufacturing and drug formulationDigital health registries and data linkageAssistive robotics for elderly care
Analysis note: Profile based on 7 projects — enough to identify clear expertise areas but insufficient to confirm long-term strategic direction with high confidence. The pharmaceutical and regulatory pivot (ORBIS, MDOT) could reflect individual faculty interests rather than institutional strategy. Third-party role in IMPROVE-PD suggests limited direct involvement in that project.