6^th Annual European Medical Device & Diagnostic
Post-Market Proactive Surveillance & Vigilance Conference

We Interact together. Innovate together. Inspire together.

POST-MARKET SURVEILLANCE & POST-MARKET VIGILANCE

The 6^th Annual European Medical Device and Diagnostic Proactive Post-Market Surveillance Conference is an interactive knowledge-sharing platform that will provide strategies for developing effective & well-integrated proactive measures to enhance PMS systems. Early implementation of proactive measures will help satisfy regulatory requirements, achieve a competitive edge, and reduce the tangible costs of downstream field corrective actions. Delving into the EU MDR & IVDR – this two-day conference will unearth some of the best strategies for PMCF activities, leveraging patient surveys, creating compliant PSURs, trend reporting, demonstrating risk-benefit ratio, creating an effective feedback loop for product improvement, and much more.

Presentations supported with real-life case studies and practical examples will provide deeper insight into smart strategies for proactive PMS. This conference will allow attendees to participate in highly interactive sessions 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 to enhance the end-to-end management of PMS whilst complying with the MDR & IVDR. Receive the actionable takeaways necessary to achieve your goals and improve proactive PMS.

POST-MARKET SURVEILLANCE & POST-MARKET VIGILANCE

The 6^th Annual European Medical Device and Diagnostic Proactive Post-Market Surveillance Conference is an interactive knowledge-sharing platform that will provide strategies for developing effective & well-integrated proactive measures to enhance PMS systems. Early implementation of proactive measures will help satisfy regulatory requirements, achieve a competitive edge, and reduce the tangible costs of downstream field corrective actions. Delving into the EU MDR & IVDR – this two-day conference will unearth some of the best strategies for PMCF activities, leveraging patient surveys, creating compliant PSURs, trend reporting, demonstrating risk-benefit ratio, creating an effective feedback loop for product improvement, and much more. Presentations supported with real-life case studies and practical examples will provide deeper insight into smart strategies for proactive PMS. This conference will allow attendees to participate in highly interactive sessions 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 to enhance the end-to-end management of PMS whilst complying with the MDR & IVDR. Receive the actionable takeaways necessary to achieve your goals and improve proactive PMS.

TT PMSV PAST SPEAKERS

Dr Yu Jin

Global Clinical and Regulatory Affairs Manager

NOTIFIED BODY 1639, SGS, BELGIUM

Dr Maria Karakitsou

UK Clinical Expert - Medical Devices

NSAI

Dr Ivan Stoyanov

In-House Clinician

NOTIFIED BODY 1639, SGS, BELGIUM

Arite Wildau

Director Patient Safety

BIOTRONIK

Stephanie Berger

Director Q&R DXR

PHILIPS HEALTHCARE TECHNOLOGY LTD

Ate Loonstra

Director Clinical Evaluation & Studies

ELEKTA

Markus Pöttker

Post-Market Surveillance Lead

SMITH & NEPHEW

Katharina Socher

Head of Product and Post-Market Excellence

SIEMENS HEALTHINEERS

Dr Sharon Perez

Vice President, Global Medical Safety

NOVOCURE

Dr Ruben Roijers

Post Market Surveillance Manager, Q&R

PHILIPS HEALTHCARE

Shokoufeh Khodabandeh

Head of Post-Market and Risk Management

STRAUMANN

Fayez Abou Hamad

MD Vigilance Expert

TERUMO EUROPE

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.