EAP Launches “The Children’s Health Pledge 2019” Campaign

April 22, 2019

On the week of the 22nd of April 2019, EAP will launch its “The Children’s Health Pledge 2019” campaign. Running until the 21st of May 2019, the campaign will urge running European Parliament elections candidates to sign EAP’s Pledge and, thus, make the health of children and young adults a European priority. In particular:

  1. Better training and information on vaccination for health professionals across Europe.
  2. Better antibiotics and more training for antimicrobial stewardship (AMS)
  3. More complete data on the state of health of Europe’s children and young adults
  4. More funding for paediatric research
  5. Stronger rules and more funding to fight childhood obesity
  6. Patient centred health care for migrant infants, children and young adults.

 

 

We encourage all our members, like-minded organisations and readers to share the Pledge among their networks; encourage their MEPs to sign it; and join our campaign on social media under the hashtag #EP4ChildHealth.

Your Enquiries Are Welcome

We will respond to you by Email

Core-MD Project

Coordinating Research and Evidence for Medical Devices (CORE-MD)

New ways to test high-risk medical devices.

 

Manufacturers of medical devices need to test their products before being allowed to market them. Specifically, they require clinical data showing their medical device is safe and efficient. In this context, the EU-funded CORE-MD project will translate expert scientific and clinical evidence on study designs for evaluating high-risk medical devices into advice for EU regulators. The project will propose how new trial designs can contribute and suggest ways to aggregate real-world data from medical device registries.


It will also conduct multidisciplinary workshops to propose a hierarchy of levels of evidence from clinical investigations, as well as educational and training objectives for all stakeholders, to build expertise in regulatory science in Europe. CORE–MD will translate expert scientific and clinical evidence on study designs for evaluating high-risk medical devices into advice for EU regulators, to achieve an appropriate balance between innovation, safety, and effectiveness. A unique collaboration between medical associations, regulatory agencies, notified bodies, academic institutions, patients’ groups, and health technology assessment agencies, will systematically review methodologies for the clinical investigation of high-risk medical devices, recommend how new trial designs can contribute, and advise on methods for aggregating real-world data from medical device registries with experience from clinical practice The consortium is led by the European Society of Cardiology and the European Federation of National Associations of Orthopaedics and Traumatology, and involves all 33 specialist medical associations that are members of the Biomedical Alliance in Europe.

EAP Representative: