Informace o projektu
Building an ecosystem for better monitoring and communicating of medication safety in pregnancy and breastfeeding: validated and regulatory endorsed workflows for fast, optimised evidence generation
(ConcePTION)
- Kód projektu
- 821520
- Období řešení
- 4/2019 - 12/2024
- Investor / Programový rámec / typ projektu
-
Evropská unie
- Horizon 2020
- Innovative Medicines Initiative
- Fakulta / Pracoviště MU
- Ústav výpočetní techniky
- WWW stránky projektu
- https://www.imi-conception.eu/
- Spolupracující organizace
-
Université de Genéve
Katholieke Universiteit Leuven
University of Manchester
University of Ulster
University of Oslo
Universita di Bologna
Uppsala universitet
Universita degli studi di Ferrara
University Medical Center Utrecht
- Odpovědná osoba Miriam Sturkenboom
INSERM
Centre hospitalier universitaire vaudois
St Georges, University of London
Academisch Ziekenhuis Groningen
BBMRI-ERIC
Consiglio Nazionale Delle Ricerche
National Institute for Public Health/and the Environment
ConcepTION partners have united around a shared vision that we have a societal obligation to radically and rapidly reduce uncertainty about the safety of medication use in pregnancy and lactation.
What do we deliver? ConcepTION aims to create a paradigm shift in how we study medication safety in pregnancy. We will establish (1) a successful, sustainable open-science based EU non-proprietary ecosystem of public and private stakeholders, pregnant women and researchers to generate and disseminate timely and reliable evidence on drugs across maternal, neonatal and long term outcomes of medication exposure in pregnancy and breastfeeding (2) a catalogue with fully characterized data sources for rapid selection of suitable data sources; 3) operational, business, network, information and data governance models, (4) quality assured and tested methodological approaches, analytical tools and data platforms
allowing for distributed analyses, (4) procedures and tools for collection of digital data and samples directly from pregnant women, (6) In vitro, in silico and in vivo models for prediction of drug transfer in human milk, (7) a biobank and analytical network for quantification of drug in human milk, (8) best practice documents endorsed by regulators and health authorities and (9) a web-based drug information knowledge bank.
How do we deliver? (1) Experienced leaders, able to manage challenging networks and public-public or public-private partnerships. (2) Defragmentation by connecting all key stakeholders and EU networks in this area. (3) Re-use of data, tools and foreground from prior European commission funded projects. (4) Connecting to leaders of similar initiatives in the USA, Canada, Asia and other parts of the world. (5) Systematic consensus & endorsement building. (6) Quality throughout as a precondition to trust the results and information by all users.