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Beyond CE marking: why MedTech access challenges differ across sectors
This panel discussion from The MedTech Forum 2026 explores how reimbursement, procurement, and evidence pathways shape access and adoption across Europe’s MedTech sectors.
Zhen Nie, Head of Med Devices, Global Consulting, IQVIA MedTech
Rob Haslewood, Global Marketing Associate Director, IQVIA MedTech
May 27, 2026

At The MedTech Forum 2026 in Stockholm, Sweden, one message stood out during the panel discussion titled “Do all MedTech sectors face the same funding and access challenges?”: innovation alone is not enough. Across Europe, many medical technologies still struggle to reach patients—not because of limited clinical value, but because healthcare systems are not evolving quickly enough to support adoption.

Moderated by Zhen Nie, Head of Med Devices at IQVIA MedTech, the session brought together:

  • Nadine Jamous, Director, EMEA Market Access, Health Economics & Reimbursement at Zimmer Biomet
  • Andrea Keady, Market Access & Reimbursement Manager at Solventum
    Chair of MedTech Europe Wound Care Sector Group
  • Aline Topouchian, Market Access and HEOR Director - EMEA at Terumo Europe Interventional Systems

Together, they explored how reimbursement, procurement, and evidence requirements vary significantly across MedTech sectors—including robotics, cardiovascular technologies, and wound care—and why some innovations scale successfully while others struggle to move beyond CE marking and pilot adoption.


The challenge: systems designed for the past

A key theme throughout the discussion was that many reimbursement and HTA frameworks still focus narrowly on clinical endpoints, without fully recognizing broader operational and workforce benefits.

Speaking about robotic-assisted surgery in orthopedics, Nadine Jamous highlighted the need to evaluate technologies more holistically:

Most technology assessments only focus on the benefit to the patient, but it’s now the time to look beyond the patient.
Nadine Jamous
Director, EMEA Market Access, Health Economics & Reimbursement, Zimmer Biomet

She explained that technologies such as robotics can improve operating room efficiency, optimize resource allocation, and support healthcare professionals—critical advantages at a time of workforce shortages across Europe. Yet despite growing recognition of these benefits, current funding systems often lack the flexibility needed to support adoption at scale or generate the evidence required to accelerate reimbursement decisions.

The discussion also touched on the challenge of timing. By the time evidence is generated and reviewed, technologies have often already evolved—making traditional assessment cycles increasingly difficult to align with innovation timelines.


Moving beyond price toward broader value

From the cardiovascular perspective, Aline Topouchian emphasized that minimally invasive technologies often create value far beyond the procedure itself, reducing hospital stays, accelerating recovery, and supporting more efficient care delivery.

She argued that procurement and reimbursement systems must evolve to better recognize this broader impact:

We need to shift the focus from only the price to broader value dimensions.

Aline Topouchian

Head of Market Access and Health Economics & Outcomes Research (HEOR), Terumo Europe

The panel discussed several examples of innovative funding and access models already emerging across Europe, including coverage with evidence generation programs in Germany and innovation-focused reimbursement pathways in France. Temporary reimbursement models for digital health technologies were also highlighted as examples of more adaptive approaches that support innovation while evidence continues to mature.

At the same time, Aline stressed that these remain fragmented examples rather than the norm across Europe. Innovation in products must be matched by innovation in healthcare systems themselves—including reimbursement, procurement, and HTA processes.


Outcomes-based care could transform access

Andrea Keady brought a wound care perspective to the discussion, arguing that healthcare systems continue to reward activity rather than outcomes:

If we had outcome-based wound care, the whole scenario would be very, very different.

Andrea Keady

EMEA Market Access Manager, Solventum

Chair of MedTech Europe Wound Care Sector Group

She explained that today’s reimbursement models often incentivize repeated interventions rather than faster healing, even when more effective approaches could improve patient outcomes while reducing system costs.

Andrea shared several powerful examples of local best practice already demonstrating what better-aligned pathways can achieve:

  • In the UK, the Manchester Amputation Reduction Strategy (MARS) brought together vascular surgeons, diabetes specialists, wound care teams, and broader multidisciplinary stakeholders to reduce avoidable amputations by nearly half within five years. The model has expanded across Manchester, but scaling nationally remains difficult.
  • In Spain, a telemedicine wound care program reduced time to wound closure by more than a month and cut hospital referrals by over 50%, generating savings of nearly €2,000 per patient.
  • In Finland, data showed that when differential diagnosis was implemented within four weeks, over 55% of wounds healed within three months. Where diagnosis was delayed beyond 12 weeks, healing rates dropped to zero.

For Andrea, these examples demonstrate that the evidence and solutions already exist.

The challenge is creating pathways that allow them to scale consistently across health systems, rather than remaining isolated pockets of success driven by individual clinical champions.


Real-world evidence and collaboration are essential

Across all sectors, the panel agreed that real-world evidence (RWE) will play an increasingly important role in demonstrating not only clinical benefit, but also operational efficiency, workforce impact, and long-term healthcare sustainability.

The session also highlighted the need for stronger collaboration between manufacturers, providers, policymakers, HTA bodies, and clinical societies. No single stakeholder can solve these challenges alone, and progress will require shared responsibility across the healthcare ecosystem.

As moderator Zhen Nie noted during the discussion, many best practices already exist across Europe. The next challenge is creating more predictable, flexible, and value-oriented pathways that allow innovation to scale more effectively and reach patients faster.


Final takeaway

While MedTech sectors face different funding and access challenges, the discussion highlighted a common underlying issue: healthcare systems are evolving more slowly than innovation itself.

The panel reinforced the need for more flexible, value-based pathways that better recognize operational efficiency, workforce impact, and long-term system sustainability—not just traditional clinical endpoints or upfront cost.

The good news is that many solutions are already visible across Europe. The challenge now is scaling them more consistently to ensure innovative technologies can move beyond CE marking and deliver meaningful value to patients and healthcare systems alike.

Learn more about how IQVIA MedTech can support you
To learn more about how IQVIA MedTech supports market access, evidence generation, and commercialization strategies across the MedTech landscape, click the CONTACT US button to reach out to Zhen Nie and the IQVIA MedTech team to continue the conversation.

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