Enhancing Health Technology Assessment Transparency through Digital Innovation

By João L. Carapinha

April 30, 2026

health technology assessment

Portugal’s national medicines agency is using digital innovation to bring greater openness to health technology assessment. INFARMED, I.P. has released a new public platform called “Tracker de Processos” that allows anyone to follow, in real time, the progress of funding and reimbursement applications for medicines within the National Health Service (SNS). The beta-version tool is updated daily and displays the status of every health technology assessment from submission to the regulator’s proposed decision.

Real-Time Visibility for All Stakeholders

The Tracker de Processos addresses long-standing information gaps by pulling live data from the Sistema de Informação para a Avaliação das Tecnologias de Saúde (SIATS). Users can track individual applications through clinical evaluation, economic evaluation, negotiation, and final proposal stages. Covering all medicine funding requests submitted or concluded after 1 January 2026, the platform excludes medical devices but offers both ongoing and completed processes. By providing daily updates and inviting feedback from patients, clinicians, industry, and the public, INFARMED is fostering accountability and predictability rarely seen among European HTA bodies.

How Portugal’s HTA Process Works

Portugal’s health technology assessment framework remains the cornerstone for deciding which medicines the SNS will finance. After EU marketing authorisation, companies submit a funding application that undergoes systematic review: first a comparative clinical assessment, then an economic evaluation examining cost-effectiveness and budget impact, followed by negotiation to safeguard the sustainability of public resources. Only once these stages are complete does INFARMED issue a proposed decision for final approval by the Ministry of Health. Parallel Early Access Programmes (PAP) enable selected medicines to reach patients before formal reimbursement when urgent clinical need exists. The Tracker makes each of these steps visible to the public.

Strategic Benefits for Patients, Industry and Policy

By shining a light on health technology assessment timelines and milestones, the new platform reduces uncertainty for manufacturers, supports better forecasting, and enables patient organisations to anticipate when innovative therapies may become available. For health economics and outcomes research teams, the standardised public data open opportunities for benchmarking and process optimisation. The beta launch combined with an open call for stakeholder input also positions Portugal as a forward-looking example of collaborative, digital modernisation in European reimbursement systems.

(Source: INFARMED launches Tracker de Processos)

Reference url

Recent Posts

medtech market access strategy
Prioritizing a Comprehensive Medtech Market Access Strategy Through Stakeholder Engagement

By João L. Carapinha

June 9, 2026

An effective medtech market access strategy must begin at the concept stage by simultaneously addressing patient needs, clinical workflows, regulatory requirements, and payer expectations rather than defaulting to FDA clearance as the sole priority. Startups that ignore this broader view risk bui...
HIV Weekly Treatment Options
Potential for Advancements in HIV Weekly Treatment Options

By João L. Carapinha

June 9, 2026

HIV Weekly Treatment Options took a major step forward as Gilead and Merck reported that their investigational once-weekly combination of islatravir and lenacapavir successfully met the primary endpoint in two Phase 3 trials. The oral regimen maintained viral suppression in adults already control...
Tovorafenib clinical assessment
Tovorafenib Clinical Assessment Outcomes and Methodological Challenges

By João L. Carapinha

June 9, 2026

The Tovorafenib clinical assessment conducted under the EU Joint Clinical Assessment process has exposed critical shortcomings in the evidence base for treating BRAF-altered pediatric low-grade glioma. Despite the therapy’s potential, reviewers concluded that robust comparative data is absent for...