Evidence map›Paper›PMID 39990182›Full record

ArticleJournal of market access & health policy2025

The EU Health Technology Assessment Regulation Halo Effect: Are Cross-Functional Teams Ready?

Sian Tanner, Rebecca Coady, Ana Lisica, Edel Falla, Anke van Engen

Abstract read
In one paragraph

Article in Journal of market access & health policy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Sian TannerIQVIA, 1101 CT Amsterdam, The Netherlands; anke.vanengen@iqvia.com.
Rebecca CoadyIQVIA, London W2 1AF, UK; rebecca.coady@iqvia.com (R.C.); ana.lisica@iqvia.com (A.L.); edel.falla@iqvia.com (E.F.).
Ana LisicaIQVIA, London W2 1AF, UK; rebecca.coady@iqvia.com (R.C.); ana.lisica@iqvia.com (A.L.); edel.falla@iqvia.com (E.F.).ORCID https://orcid.org/0000-0002-9673-402X
Edel FallaIQVIA, London W2 1AF, UK; rebecca.coady@iqvia.com (R.C.); ana.lisica@iqvia.com (A.L.); edel.falla@iqvia.com (E.F.).ORCID https://orcid.org/0000-0002-9179-682X
Anke van EngenIQVIA, 1101 CT Amsterdam, The Netherlands; anke.vanengen@iqvia.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The focus of manufacturers preparing for implementation of the EU HTA Regulation (HTAR) in 2025 has understandably been on their market access teams, and how they can be best equipped to adapt to this significant change. Considering the critical nature of market access in ensuring innovation reaches patients, it should be no surprise that the EU HTAR will have impacts far beyond this function. Here, we utilize published EU HTAR guidance, a pragmatic literature review, internal analysis, and insights from engagements with manufacturers, to outline some of the key cross-functional considerations arising from JSC and JCA, and how manufacturers should account for these in their EU HTAR readiness plans.

Indexed as

EU HTA initiativeEU HTA processEU HTA regulationEuropean Access AcademyEuropean Access EnvironmentHTA bodiesHTA communityHTA proceduresinnovative health technologiesMarket Access Societypatient access

Identifiers

PMID39990182
PMCPMC11843822

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.