TEDDY Network joins to Discuss Emerging Paediatric Clinical Trial Standards and Global Best Practices The TEDDY Network is delighted to highlight its involvement in the upcoming EPTRI webinar: “CONSORT- and SPIRIT-Children: Reflections on...
TEDDY Stichting Officially Founded to Advance Paediatric Research Across Europe
TEDDY Network and TEDDY Stichting Unite to Promote Excellence in Paediatric Research in Europe On January 12, 2026, TEDDY Stichting was officially established in Zoetermeer, the Netherlands. The Foundation is...
TEDDY Partners with Curewiki to Empower Patients Through the Patient Voice Database
A Secure, GDPR-compliant platform to enable meaningful patient participation in clinical research TEDDY Network has integrated the Patient Voice Database into the TEDDY website. This secure, patient-centred, research-oriented platform developed...
2nd ERDERA Training for Young Advocates for Rare Diseases
ERDERA opens call for young rare disease advocates to join training in Paris The TEDDY- European Network of Excellence for Paediatric Clinical Research is proud to announce the second edition of the young advocates’ training organised under the framework of...
Strengthening Paediatric Research: TEDDY Contributes to New Trial Guidelines
Global Guidelines for Paediatric Trials Developed with TEDDY Expertise TEDDY is proud to announce the involvement in the preparation of major guidelines aimed at improving the design, and reporting of paediatric clinical trials. The...
Advancing the Future of Paediatric Research: TEDDY Network at the Global Forum in Geneva
TEDDY Network’s contributions to child engagement and evidence-based paediatric medicine at a global scientific event The TEDDY Network is proud to announce that two abstracts have been accepted for poster presentation at the international congress “Paediatric...
Eirini Daskalopoulou joins Global Network for Rare Disease (GNRD)
Eirini Daskalopoulou’s Role in Shaping Global Rare Disease Care Pathways Rare Diseases International, in collaboration with Rare Care Centre and Wilhelm Foundation, is launching a Working Group to develop a Model Care Pathway for Rare Diseases adaptable to different...
“Raising Youth Voices”: Empowering the Next Generation of Rare Disease Advocates
“Raising Youth Voices” Launches Global Platform for Young Rare Disease Advocates TEDDY Network is pleased to highlight the launch of “Raising Youth Voices,” a new global initiative coordinated by Rare Disease Day that seeks to ensure young people living with rare...
TEDDY Contributes to Groundbreaking Article on Transparent Reporting of Paediatric Trial Interventions in Pediatrics
Advancing Paediatric Clinical Research Reporting with TEDDY’s Expertise TEDDY is proud to announce its contribution to a significant article titled "Transparent Reporting of Pediatric Clinical Trial Interventions: TIDieR-Children and Adolescents", recently published...
Renewal of the JRU–EPTRI-IT Agreement: Strengthening the Italian Paediatric Research Node
TEDDY Coordinates the Future Growth of Italy’s Paediatric Research Infrastructure TEDDY- European Network of Excellence for Paediatric Clinical Research is pleased to announce the renewal of the Joint Research Unit (JRU) – EPTRI-IT Agreement, marking an important...