Spread the Word

Take the Mock Exam

25 minutes | 15 multiple choice questions

Curious? Take the Mock Exam, designed to simulate the real testing experience. Create a profile to access the mock exam here

If you have any questions please contact us on [email protected].

How can you help?

This page provides essential promotional tools to help spread the word about the EBP-EAP exam among members of your national society , colleagues, and broader network. 

Spread the news in your country in the following ways:

  • Flyers (feel free to add this on a notice board).
  • Sending this email to your students/trainees in your network. 
  • Add these PowerPoint slides at the end of any presentation. 
  • Social Media: Use our custom made posting plan with posts and accompanying images to share the news! To download any images, simply click on the link under the image in the posting plan. 
  • Alternatively, follow EAP on social media to spread the word by sharing. We are on FacebookInstagramLinkedIn and X. Send us your details and we will follow you back.

Click on the links below for easy access to the promotional tools.

What to Expect
on Exam Day

Exam Proctoring

Your Online Invigilator

During the ONLINE exam, ProctorU, an expert in remote exam invigilation, will actively monitor the exam session. The invigilator ensures smooth progress and assists with technical issues while monitoring the exam. Please note that your camera and microphone must remain active throughout the exam, and your awareness and consent for monitoring are crucial. This requirement aligns with GDPR guidelines, ensuring data protection. All exam applicants should be aware of and agree to this necessity.

To learn more, watch this video: https://meazurelearning.wistia.com/medias/x8sicg86fm.

Your Enquiries Are Welcome

We will respond to you by Email

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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: