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From Approval to Access and Adoption: Leveraging Real-World Data for Medical Devices
Collection of data in the real world is ubiquitous. Some of the medical device vendors fully utilize this trend while others are in the early stages of exploring how different data sources can support different use cases throughout the medical devices lifecycle.
Real-world data (RWD) and evidence (RWE) can add new and supplementary insights on the performance of medical devices outside of the rigorously controlled confines of clinical trials. Additionally, the longitudinal nature of much of this data can provide greater insights into the safety and longer-term needs of patients. Furthermore, real-world data can support evidence on the fit-for-purposeness across additional use cases, not studied in early trials. Data collected in a real-world setting can serve to initiate a feedback loop, whereby providers and hospitals receive evidence that can serve to improve clinical practice.
Join this roundtable in collaboration with S3 Connected Health, for which we will delve into three specific phases of the lifecycle and explore pragmatic considerations on leveraging RWD/RWE most effectively:
- Regulatory Approval: What types of real-world data are available for medical devices, and how can they be leveraged to improve patient outcomes?
- Market access: How can real-world data/evidence be used to support health technology assessment (HTA) and market access for medical devices, and what are the key considerations for payers and providers?
- Adoption and implementation: How can real-world evidence be used to support the adoption of medical devices by patients and integration into clinical workflows, and what are the key challenges and opportunities?
We would like to remind you that our meetings are small and intimate sessions with a limited number of seats available, therefore we rely on your attendance and participation to ensure a high quality and valuable meeting for all. If you are confirmed for this meeting we ask if you can please ensure your attendance on the day.
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From Approval to Access and Adoption: Leveraging Real-World Data for Medical Devices
From Approval to Access and Adoption: Leveraging Real-World Data for Medical Devices
Join this HealthXL Event today:
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You actively participate in this discussion. Spaces are limited to 8 - 12 people, allowing you to focus on quality in-depth conversations.
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Collection of data in the real world is ubiquitous. Some of the medical device vendors fully utilize this trend while others are in the early stages of exploring how different data sources can support different use cases throughout the medical devices lifecycle.
Real-world data (RWD) and evidence (RWE) can add new and supplementary insights on the performance of medical devices outside of the rigorously controlled confines of clinical trials. Additionally, the longitudinal nature of much of this data can provide greater insights into the safety and longer-term needs of patients. Furthermore, real-world data can support evidence on the fit-for-purposeness across additional use cases, not studied in early trials. Data collected in a real-world setting can serve to initiate a feedback loop, whereby providers and hospitals receive evidence that can serve to improve clinical practice.
Join this roundtable in collaboration with S3 Connected Health, for which we will delve into three specific phases of the lifecycle and explore pragmatic considerations on leveraging RWD/RWE most effectively:
- Regulatory Approval: What types of real-world data are available for medical devices, and how can they be leveraged to improve patient outcomes?
- Market access: How can real-world data/evidence be used to support health technology assessment (HTA) and market access for medical devices, and what are the key considerations for payers and providers?
- Adoption and implementation: How can real-world evidence be used to support the adoption of medical devices by patients and integration into clinical workflows, and what are the key challenges and opportunities?
We would like to remind you that our meetings are small and intimate sessions with a limited number of seats available, therefore we rely on your attendance and participation to ensure a high quality and valuable meeting for all. If you are confirmed for this meeting we ask if you can please ensure your attendance on the day.
Participants
Participants
Piotr Sokolowski
Head of Strategy, MedTech Solutions at S3 Connected Health
Blaise Jacholkowski
Senior Business Solution Manager / Digital Health, Zuhlke Group
Marko de Jager
Principal Scientist, Philips Ambulatory Monitoring & Diagnostics
Friedrich Wetterling
Data Science and Research Manager, FIRE1
Frances Mitchell
Director, Innovation Strategy and Insight, Teleflex
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Tiffany Naidoo
Senior HEMA Manager, BIOTRONIK
Ventsislav Dobrev
Global Innovation & Digital Health Solutions Manager, Ypsomed
Yash Prajapati
Consultant, zs
Kathleen Van Vlierberghe
Vice President Healthcare Solutions & Partnerships EMEA, Boston Scientific
Aghogho Ekpruke
Innovation Leader, MedTech Architect, Medtronic
Gurdish Singh
Portfolio Asset Lead, Boehringer Ingelheim
Marc Blanchard
Chief Development Officer - CDO at ATREON SA
Abdul Khaled
Senior Director - Digital Solutions, WS Audiology
Anupama Govindarajan
Sr. Advisor to Digital Health FDA / Program Officer NIH
Sujai Kalra
Director, Analytics & Integrations, Nevro
Bradley Carlson
Consultant, Independent
Mike Pace
CEO & Founder, PalmHealth.co
Weronika Michaluk
Principal , HTD Health
Sandra Nagale
Director - Digital Health & Data Solutions, Boston Scientific
Bill Betten
Director of Solutions, S3 Connected Health
Brenna Beluk
Product Manager, Digital Health, Consultant, Boston Scientific
Up to 12
From Approval to Access and Adoption: Leveraging Real-World Data for Medical Devices
Collection of data in the real world is ubiquitous. Some of the medical device vendors fully utilize this trend while others are in the early stages of exploring how different data sources can support different use cases throughout the medical devices lifecycle.
Real-world data (RWD) and evidence (RWE) can add new and supplementary insights on the performance of medical devices outside of the rigorously controlled confines of clinical trials. Additionally, the longitudinal nature of much of this data can provide greater insights into the safety and longer-term needs of patients. Furthermore, real-world data can support evidence on the fit-for-purposeness across additional use cases, not studied in early trials. Data collected in a real-world setting can serve to initiate a feedback loop, whereby providers and hospitals receive evidence that can serve to improve clinical practice.
Join this roundtable in collaboration with S3 Connected Health, for which we will delve into three specific phases of the lifecycle and explore pragmatic considerations on leveraging RWD/RWE most effectively:
- Regulatory Approval: What types of real-world data are available for medical devices, and how can they be leveraged to improve patient outcomes?
- Market access: How can real-world data/evidence be used to support health technology assessment (HTA) and market access for medical devices, and what are the key considerations for payers and providers?
- Adoption and implementation: How can real-world evidence be used to support the adoption of medical devices by patients and integration into clinical workflows, and what are the key challenges and opportunities?
We would like to remind you that our meetings are small and intimate sessions with a limited number of seats available, therefore we rely on your attendance and participation to ensure a high quality and valuable meeting for all. If you are confirmed for this meeting we ask if you can please ensure your attendance on the day.
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From Approval to Access and Adoption: Leveraging Real-World Data for Medical Devices
From Approval to Access and Adoption: Leveraging Real-World Data for Medical Devices
From Approval to Access and Adoption: Leveraging Real-World Data for Medical Devices
Collection of data in the real world is ubiquitous. Some of the medical device vendors fully utilize this trend while others are in the early stages of exploring how different data sources can support different use cases throughout the medical devices lifecycle.
Real-world data (RWD) and evidence (RWE) can add new and supplementary insights on the performance of medical devices outside of the rigorously controlled confines of clinical trials. Additionally, the longitudinal nature of much of this data can provide greater insights into the safety and longer-term needs of patients. Furthermore, real-world data can support evidence on the fit-for-purposeness across additional use cases, not studied in early trials. Data collected in a real-world setting can serve to initiate a feedback loop, whereby providers and hospitals receive evidence that can serve to improve clinical practice.
Join this roundtable in collaboration with S3 Connected Health, for which we will delve into three specific phases of the lifecycle and explore pragmatic considerations on leveraging RWD/RWE most effectively:
- Regulatory Approval: What types of real-world data are available for medical devices, and how can they be leveraged to improve patient outcomes?
- Market access: How can real-world data/evidence be used to support health technology assessment (HTA) and market access for medical devices, and what are the key considerations for payers and providers?
- Adoption and implementation: How can real-world evidence be used to support the adoption of medical devices by patients and integration into clinical workflows, and what are the key challenges and opportunities?
We would like to remind you that our meetings are small and intimate sessions with a limited number of seats available, therefore we rely on your attendance and participation to ensure a high quality and valuable meeting for all. If you are confirmed for this meeting we ask if you can please ensure your attendance on the day.
Join this group of peers and get a feel of what it's like to belong to a community of digital health gamechangers.
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What are HealthXL Virtual Meetings?
HealthXL Virtual Meetings are private group meetings limited to 10 people across different demographic and stakeholder groups. For 75 minutes, you take a deep dive into your chosen topic and explore it from different angles. Virtual Meetings are not webinars: There is no audience, no recording and no hiding behind a screen. You actively participate in a discussion to solve your present challenges and design the future of digital health. And through our Community Hub, you stay up-to-date on the latest news and insights, allowing you to fully immerse yourself in the topic before, during and after.
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HealthXL brings together gamechangers of digital health to support honest discussions in small, private groups. In our Community Hub, for which you can register for free, you can follow a wide range of communities across telehealth, digital therapeutics, patient engagement and more. As a full HealthXL member, you also get access to curated news, the latest insights and an expert network to connect with. Join exclusive virtual meetings to exchange strategies, viewpoints and learnings with members from like-minded yet diverse stakeholder groups.
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As member of HealthXL, you join a community of digital health thought leaders, innovators and game changers around the world. With your membership, you get access to hundreds of insights, reports and resources. You can browse a database with over 90k healthcare organizations and view their active strategic partnerships, commercial relationships, latest funding rounds and research. Through our in-house curated digital health newsfeed, you stay informed on the most impactful news and you can regularly meet with members to share learnings, discuss the latest developments and connect with peers of different demographical stakeholder groups. Contact us today to find out about pricing options.
Through focus groups, we bring together 6-10 thought leaders and industry stakeholders in a series of virtual meetings to collaborate around a defined topic. Each meeting gives the group the opportunity to examine, analyze and collaborate with one another around a digital health topic as well as produce a shareable result.
