Spotlight on a National Hub: Greece
HELPnet (Hellenic Paediatric Network) is the Greek National network of paediatric clinical research sites.
CDISC Public Review: Paediatrics User Guide
In collaboration with c4c, CDISC is developing a Paediatrics User Guide which is now available for public review.
Spotlight on a National Hub: Danish
DanPedMed is the Danish National Hub in the connect4children (c4c) project and is represented as a third party to the c4c beneficiary HUS-Norway. DanPedMed is working towards becoming an independent Danish National Hub, after the initial c4c IMI funding period concludes in 2024. DanPedMed was established in 2016 through a collaboration between Danish Pediatric Society…
“Networking to improve pediatric research”
On 27th May 2022, the STAND4Kids National Hub is organizing an online event “Networking to improve pediatric research”.
c4c team presentation post: Alessio Ceccherelli
Meet the team behind c4c! We are a diverse group of people from many different backgrounds, but all of us are working towards a common goal: better medicines for children through European clinical trials. Today’s spotlight is on Alessio Ceccherelli from the Tor Vergata University of Rome, who manages the c4c Academy learning platform. The…
New c4c webinar for patients!
c4c is hosting an online webinar on 28th April from 6pm to 7:30 pm CET to explain how patients have been engaged within the c4c project.
Calling for an International Law Firm to support c4c!
A call for tender for subcontracting a “Specialised International Law or Consultancy Firm or Legal Advisor” is open until June 3rd 2022.
Spotlight on a National Hub: Norway
NorPedMed is the Norway National Hub in c4c, and the secretariat has been strengthened accordingly with additional resources allocated to take care of our obligations within the c4c. NorPedMed was founded in 2013 to link the paediatric Clinical Trial Units (CTUs) at the six university hospitals. The basic infrastructure of these CTUs (e.g., nurses, housing,…
c4c outreach to patient advocates nationally
c4c outreach to patient advocates nationally- Webinar for the Dutch EUPATI-NL community VSOP, the Dutch Patient Alliance for Rare and Genetic Diseases, is participating in the c4c cross-cutting team for Patient and Public Involvement (PPI), which is working on implementation of patient and public involvement activities across Europe. VSOP was invited by the EUPATI-NL project…
c4c team presentation post: Sofia Jacob
Meet the team behind c4c! We are a diverse group of people from many different backgrounds, but all of us are working towards a common goal: better medicines for children through European clinical trials. Today’s spotlight is on Sofia Jacob, who oversees multiple activities within c4c to ensure they are completed in time. Sofia…