European Medical Device Safety & Compliance Conference

World’s Greatest minds in drug safety, pharmacovigilance, data analysis, reporting, government policy, and innovative technology.

key information

OUR STORY TO TELL THE WORLD

OUR CONFERENCE PROGRAM

We are trying to create a platform for opening new topics or troubling issues and create a safe space for a stimulating, inspiring, and fruitfull discussion about current trends and challenges in the field of medical device safety. Don’t miss this great opportunity to be part of this event, to connect with the specialists in the field and share your ideas and insights!

Main Takeaways

You will hear experts talk about the current issues in this ever-evolving industry. The best practice case studies on value added medicines opportunities and how it evolves to mature portfolio management organizations.
What is the role of project management in different levels of maturity of ppm in different organizations?
How to prioritize projects, what methodologies to use for risk and decision analysis?

Building a top notch alliance network, working with behavior of internal stakeholders in project portfolio management.
Considering factors for being a day 1 or first to market with complex generics and combination products.
Working with innovation, utilizing internal cooperation to ensure successful product launch, considering ip strategies for generics and biosimilars, working with mature products, working with emerging markets.

Testimonials

“Great dialogue on key issues. Everyone shared truthful insight and did not hold back, even on negative experiences.”

Sameer Thapar

Assistant Professor & Advisor

“High-quality speakers and attendees, a great mix between healthcare providers, life science companies, providers of digital health & AI solutions, and investors.”

John Mulcahy

CEO, HealthGenuity

“Unlike some other similar events, I found relevance in every session within your conference. The content was neither too simplistic nor too advanced. The participants and presenters provided a diverse view of the issues that are present for most in this industry.”

Christine Clearwater

Healthcare Manager

“Loved it. It was very practical and provided valuable insight into practical methods that are actionable.”

Daniel Naranjo

Global Safety Lead, Global Patient Safety Evaluation, Takeda

Event Speakers

Arite Wildau

Director Patient Safety, Biotronik

Ana Mendonça

Sr. Vigilance Process Manager, Novartis

Daniel Kvak

CEO, Carebot

Dardan Uka

Global PMS and Implants/Instruments Vigilance Manager, Corin

Crystal D’Silva

Manager (Preclinical Toxicology - Quality), Baxter R&D Europe SPRL

Ariana Adjani

Co-Founder at Fine Treatment

Lea Caramma

Post-Market Surveillance Engineer, Lima Corporate

Ida Søholm

Senior Project Manager, Regulatory Affairs - Software, 3Shape

Renea Schønemann Olsen

Senior Post-Market Surveillance Manager, Scientific Affairs, 3Shape

Mette Luxhøj

Head of Regulatory Affairs, Software, 3Shape

Heinrich Martens

Vice President Regulatory Affairs, Fresenius Kabi

Leon Doorn

Head of Regulatory Compliance, Aidence

Leo Hovestadt

Director Governmental Affairs EU, Elekta

Talia Milosevic

Senior Manager, Clinical Safety, Surgical Structural Heart, Edwards Lifesciences

Maurizio Zaccheddu

Senior Quality Assurance Manager, Sonova

Fatima Bennai-Sanfourche

Senior Director of QA & RA Compliance for Medical Devices, Combination product and eHealth, Bayer AG

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AGENDA

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REGISTRATION

€ 2399

Access to All Conference Sessions
Access to Post Conference Networking
Conference Materials
Includes Coffee Breaks, Snacks and Refreshments, Seated Lunch

Present on the Main Stage
Hold an exhibit at this event
Showcase your Brand in Marketing Material
Gain exposure through alternative partnership benefits

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