Health
EU Must Simplify Rules to Boost Healthcare Innovation, Commissioner Says
Europe must simplify its healthcare regulations to strengthen competitiveness, support innovation and ensure patients gain faster access to treatment, European Health Commissioner Olivér Várhelyi said on Tuesday.
Speaking at the Euronews Health Summit in Brussels, Várhelyi described healthcare as one of the most pressing challenges facing both Europe and the wider region. He pointed to the growing burden of non-communicable diseases, shortages of healthcare workers and an ageing population as key factors putting pressure on the system.
Várhelyi said Europe’s healthcare model remains distinct and should be preserved, calling it a core strength that provides reliability for societies across the continent. At the same time, he warned that the system is under strain and cannot be taken for granted in the future without reforms.
In response to these challenges, the European Union has introduced a series of measures aimed at improving resilience and crisis response in the health sector. Várhelyi said these reforms also carry significant economic potential, with the healthcare and pharmaceutical industries playing a major role in Europe’s competitiveness.
A key development has been the overhaul of pharmaceutical rules agreed in December 2025, driven by medicine shortages and vulnerabilities in supply chains. Várhelyi said the sector accounts for about five percent of manufacturing value added and nearly 11 percent of EU exports, underlining its importance to the economy.
The updated framework is intended to modernise regulations and better support the development of advanced treatments, particularly for patients with unmet medical needs. According to Várhelyi, the reforms aim to make the regulatory system more adaptable and responsive to innovation.
Alongside this, the EU has introduced the Biotech Act, designed to make it easier for new products to move from research laboratories to large-scale production and market distribution. The Commissioner said the legislation, along with updates to medical device regulations, places simplification at its core.
He argued that existing rules often create unnecessary costs, delays and uncertainty for companies, which can slow the delivery of new treatments to patients. By streamlining procedures and improving enforcement, the EU aims to create an environment where innovation can develop more rapidly.
Várhelyi said these efforts are essential to maintaining Europe’s position in the global healthcare and technology landscape. He added that simplifying regulations would help ensure that new ideas are translated into effective treatments more quickly, benefiting both the industry and patients across the region.
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