News

TEDDY to join the EUCROF GDPR Code

TEDDY Network has been invited to join the Monitoring Body of the EUCROF Code of Conduct for Service Providers in Clinical Research. EUCROF, the European CROs Federation, is the owner of the GDPR Code which helps to ensure the privacy rights and freedoms of trial participants while promoting the lawful, fair, and meaningful use of

June 29th, 2021|

Manifesto to remark the unmet needs of non-Covid patients: TEDDY among the supporting institutions

TEDDY Network is one of the 50th associations from 18 countries signed a Manifesto with 10 Recommendations addressed to European institutions, to remark the unmet needs of non-Covid patients, launched by Active Citizenship Network (ACN) on the occasion of the recent "European Patients’ Rights Day". European Union, national and regional institutions, and decision-makers should

May 24th, 2021|

TEDDY Network members among the authors of the article “Children’s Preferences for Oral Dosage Forms and Their Involvement in Formulation Research via EPTRI ….”

The article "Children’s Preferences for Oral Dosage Forms and Their Involvement in Formulation Research via EPTRI (European Paediatric Translational Research Infrastructure)" has been published in Pharmaceutics as part of the Special Issue Scientific Highlights in the First European Paediatric Translational Research Infrastructure Open Meeting. The article is a result of the study commissioned by the

May 19th, 2021|

SARS-CoV-2 in Children, get the right scientific facts

The article ‘Susceptibility to SARS-CoV-2 infection among children and adolescents compared with adults’, published on JAMA Pediatrics, is the result of a systematic review and meta-analysis including 32 studies, children and adolescents younger than 20 years had 44% lower odds of secondary infection with SARS-CoV-2 compared with adults 20 years and older. Preliminary evidence suggests

April 28th, 2021|

Clinical Trial Regulation 536/2014

The Clinical Trials Regulation (EU) 536/2014 is foreseen to become applicable at the end of January 2022. To support Member States with its implementation, DG SANTE of the European Commission, the European Medicines Agency (EMA) and the Clinical Trials Facilitation and Coordination Group of the Heads of Medicines Agency jointly organised a training course on 9-10

April 28th, 2021|

TEDDY feedback to the Evaluation and revision of the general pharmaceutical legislation

As part of the EU pharmaceuticals strategy, and drawing lessons from the COVID-19 pandemic, the Commission launched an inception impact assessment to evaluate and revise the EU’s general legislation on medicines for human use to ensure a future-proof and crisis-resistant medicines regulatory system. TEDDY Network participated to the consultation providing its comments to be considered

April 28th, 2021|

TEDDY comments to the EU Strategy for International Cooperation in R&I

On April 9th 2021, TEDDY network provided its feedback to the European Commission public consultation on the revision of the Europe’s strategy for international cooperation in research and innovation. The current strategy for international cooperation on research and innovation between Europe and the rest of the world was set out in a Commission Communication in

April 20th, 2021|

EJP RD LAUNCHED ITS FIRST MASSIVE OPEN ONLINE COURSE – MOOC

The European Joint Programme on Rare Diseases has launched its first academic education course “Diagnosing Rare Diseases: from the Clinic to Research and back” related to diagnosis in the rare disease’s context. The course, started on April 26th, will last 5 weeks with 3 hours weekly study. In 2019 the EJP RD has launched a

April 9th, 2021|

DIAGNOSIS AND TREATMENT OF CHRONIC NEUROPATHIC AND MIXED PAIN IN CHILDREN

We are happy to inform you that the article "Diagnosis and Treatment of Chronic Neuropathic and Mixed Pain in Children and Adolescents: Results of a Survey Study amongst Practitioners" has been published in Children open access journal. The article shows the results of a questionnaire administrated to investigate the international practice amongst practitioners for the

March 23rd, 2021|

Returning Individual Clinical Trial Results Back to Patients

The VISION-DMD published a white paper on how to return individual clinical trial results back to patients. It focuses on addressing the ethical and technical challenges, using the vamorolone clinical trial experience. The VISION-DMD is a project aimed to advance and accelerate the clinical development of the orphan drug vamorolone (also known as VBP15) for

March 17th, 2021|