EAP Learning is a virtual classroom designed to support paediatric trainees and professionals in their educational journey. Accessible via mobile, tablet, or laptop, the platform offers a range of resources, including case studies, podcasts, and videos, covering different aspects of paediatrics.
Enhance your knowledge with our structured case studies, each accompanied by multiple-choice questions (MCQs), detailed explanations, and references. Available modules include:
Latest released modules:
General Paediatrics
12 cases in general paediatrics, with MCQs, case explanations and references
GI, Endocrine & ID
12 cases in GI/Endocrine/ID with MCQs, case explanations and references
Neurology, Neonatology & Surgery
12 cases in Neurology /Neonatology / Surgery with MCQs, case explanations and references
Respiratory, Oncology & ID
12 cases in Respiratory, Oncology & ID MCQs, case explanations and references
General Paediatrics II
12 new cases in General Paediatrics with MCQs, case explanations and references
Diseases of the Neonate
6 cases in diseases of the Neonate, with MCQs, case explanations and references
The EAP Learning application offers seamless access to interactive educational resources anytime, anywhere. Explore case studies specifically designed to support your EBP-EAP exam preparation, enhancing your learning experience in a way that suits your individual needs. Track your progress effortlessly across multiple devices, ensuring a consistent and personalised journey.
Simply download the application, create a profile, and purchase one or more case blocks. An activation code is required to unlock your resources and start learning immediately.
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.