Consolidated experience leading research projects with multiple stakeholders, from a very diverse range of environments and cultures.
Proven track record on
highly innovative research projects
The European Medicines Agency (EMA) is establishing a Coordination Centre to provide timely and reliable evidence on the use, safetyand effectiveness of medicines for human use, including vaccines, from realworld healthcare databases across the European Union (EU). The role of the Coordination Centre is to develop and manage a network of real-world healthcare data sources across the EU and to conduct scientific studies requested by medicines regulators and, at a later stage, also requested by other stakeholders. By supporting decision-making on medicines, a wide range of stakeholders will benefit, from patients and healthcare professionals to health technology assessment bodies, payers and the pharmaceutical industry. Additionally, DARWINEU® will provide an invaluable resource to prepare for and respond to future healthcare crises and pandemics.
The mission of the European Health Data & Evidence Network (EHDEN) is to provide a new paradigm for the discovery and analysis of health data in Europe, by building a large-scale, federated network of data sources standardised to a common data model. EHDEN will build on prior projects, such as EMIF and EHR4CR, in scaling their original intents and technologies.
The main aim of NEURONET is to set up an efficient platform to boost synergy and collaboration across the IMI projects of the Neurodegenerative Disorders (ND) portfolio, assisting in identifying gaps, multiplying its impact, enhancing its visibility, and facilitating dovetailing with related initiatives in Europe and worldwide.
Neuronet KB includes links to over 380 publications and more than 350 publishable deliverable report
This comprehensive resource is an integral part of NEURONET's endeavour to boost collaboration across the research portfolio by assisting in identifying gaps, multiplying the portfolio's impact and enhancing its visibility with related initiatives in Europe and worldwide.
ERA4TB (European Regimen Accelerator for Tuberculosis) project is a public-private initiative devoted to accelerating the development of new treatment regimens for tuberculosis. The ERA4TB platform is based on a progression pipeline that can cater simultaneously for a variety of molecules at different stages of development.
The Translational Safety Biomarker Pipeline (TransBioLine) Project aims to generate exploratory and confirmatory data supporting regulatory qualification and acceptance of novel safety biomarkers for five target organ systems (kidney, liver, pancreas, vascular, and central nervous system) for application in drug development.
SYNAPSE PI is a graphical interface based on the Business Intelligence dashboard model, that displays key documentation, metrics and day-to-day relevant information at a single glance.
The overall objective of HTx is to create a framework for next generation Health Technology Assessment that supports patient-centred, societally oriented, real-time decision-making for integrated healthcare throughout Europe.
The eTRANSAFE project aims at improving the safety assessment across the drug discovery and development process by applying bioinformatics approaches to shared preclinical and clinical data to systematically analyse the translatability of effects. Thus, enabling the optimisation of resources and the development of safer medicines.
ROADMAP aims to create the conditions for an open collaboration that yields consensual and efficient uses of RWE for the benefit of Alzheimer’s Disease patients and their caregivers. This will be achieved by using pilot studies to assess methods of data integration for patient outcomes that are useful for disease modelling; and developing tools and methods for stakeholder engagement. ROADMAP will set new standards for the collation and evaluation of RWE in Alzheimer’s Disease.