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5th Annual European Medical Device and Diagnostic Clinical Evidence Strategy Conference

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Conference Overview

The 5th Annual European Medical Device and Diagnostic Clinical Evidence Strategy Conference 2024 bring back Europe’s most important conference focussed on developing effective and integrated strategies for clinical evidence. This two-day conference will have some of the best strategies on how to implement the pre-market and post-market data, addressing the practicalities of real-world sources for clinical data collection and much more.

Presentations supported with real-life case studies and practical examples will provide deeper insight into the strategies for generating and collecting quality clinical data. This conference will provide attendees with an opportunity to participate in a highly interactive session supported by real-life business examples, case studies, Q&A sessions and roundtable discussions led by experienced professionals. First-hand experience and tips will be shared on the practicalities of conducting clinical studies within Europe – identifying the clinical data necessary for compliance with medical devices and regulations. Receive the actionable takeaways necessary to achieve your goals with a further improved clinical evidence process. You will be able to network with your peers, including leading technology innovators and service providers; the clinical evidence conference will also enable attendees to build new relationships with delegates and exchange ideas in a collaborative setting.

Our Industry Specialists

NOTIFIED BODY

EU CE_Dr. Yu Jin

Dr Yu Jin

Global Clinical and Regulatory Affairs Manager

NOTIFIED BODY 1639, SGS, BELGIUM

PMSV-BW-Website-Speaker-Image-Dr-Ivan-Stoyanov.png

Dr. Ivan Stoyanov

In-house Clinician

SGS

Andriani Daskalaki

Dr. Andriani Daskalaki

Clinical Expert/Regulatory (MDR)

MDC MEDICAL DEVICE CERTIFICATION GmbH

Gavin

Gavin Quigley

Senior Internal Clinician

BSI

Dr Marianna Mastroroberto

Dr. Marianna Mastroroberto

Internal Clinical Expert

KIWA CERMET ITALIA (NB 0476)

Bevilacqua Francesca

Bevilacqua Francesca

IVD Team Leader

TÜV SÜD

Daniele Bollati

Daniele Bollati

IVD Product Conformity Assessment/Medical Devices Expert

IMQ

EU CE_Silvia Busoli Badiale

Silvia Busoli Badiale

Lead auditor and product reviewer of non-active medical devices and substance-based medical devices

IMQ

Benedicte Nuyttens

Benedicte Nuyttens

Scientific File Manager

FEDERAL AGENCY FOR MEDICINES AND HEALTH PRODUCTS

Ing.Nebojsa Serafimovic

Assessor Medical Devices, Senior Expert

AUSTRIAN MEDICINES AND MEDICAL DEVICE AGENCY

Targeted Content

With our targeted attendee and speaker line-up, you can have meaningful conversations with industry-specific experts who have faced the same situations and challenges. Spark new ideas by brainstorming during our breakout sessions, informal post-session Q&As, panel debates, case studies, and workshops.

Meet Industry Leaders

Our robust screening process ensures an exclusive environment where you can focus on connecting and fostering stronger working relationships with those in the medical device field. Collaborate to find the necessary solutions to your current problems.

Customize Your Content

Get the most out of this event experience by choosing what content is most relevant for you and your company and tailoring your event experience around this decision. Learn and connect with whomever you want, whenever you want, and however you want.

If you are a part of the Medical Device Clinical Evidence community, TT Clinical Evidence guarantees a valuable return on time invested.

Past Partners

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