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EBP-EAP Exam: Practical Information and Mock Exam

This page provides essential practical information to help you prepare for the exam day and includes access to a special Mock Exam designed to simulate the real online testing experience.

Click the button below to begin your Mock Exam. You will be asked to create a free account on the exam platform before accessing the questions.

 

  • If you have already registered for the EBP-EAP Exam, use the same login credentials.
  • If not, you can create a new account with a username and password.
  • A verification code will be sent to your email; enter this code to confirm your account.

 

Once logged in, scroll down to access the Mock Exam. You will be presented with 15 multiple-choice questions, which you can complete in 25 minutes.

What to Expect
on Exam Day

  • Number of Questions: ~120 multiple-choice questions
  • Duration: 2 hours
  • Content: Covers a broad range of paediatric essential clinical knowledge
  • Format: Online, proctored, scenario-based MCQs
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To learn more, watch this video: https://meazurelearning.wistia.com/medias/x8sicg86fm.

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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:

  • BERTHOLD KOLETZKO
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