Evidence map›Paper›PMID 40715747›Full record

ArticleTherapeutic innovation & regulatory science2025

Incorporating Patient Needs and Perspectives in Additional Risk Minimization Measures and Other Pharmacovigilance Deliverables - A Framework and Implementation Roadmap.

Linda Smeding, Robert Massouh, Farai Moyo, Marilyn Metcalf, Shannon Altimari, Ekaterina Edle von Dall'Armi, Elisa Formenti

Abstract read
In one paragraph

Article in Therapeutic innovation & regulatory science, 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

7 authors.

Linda SmedingGSK, Avenue Fleming 20, Wavre, 1300, Belgium. linda.x.smeding@gsk.com.
Robert MassouhGSK, London, UK.
Farai MoyoGSK, London, UK.
Marilyn MetcalfGSK, Philadelphia, USA.
Shannon AltimariGSK, Baar, Switzerland.
Ekaterina Edle von Dall'ArmiGSK, Munich, Germany.
Elisa FormentiGSK, Verona, Italy.

Funding

GSK N/A
6 · The paper itself

Abstract

Various initiatives and guidelines exist to support patient engagement (PE) throughout the lifecycle of a medicinal product. While the recent European Medicines Agency guideline on good pharmacovigilance practices (Module XVI; Revision 3) reinforces the importance of involving patients to create effective risk minimization strategies, frameworks supporting the systematic adoption of PE by Marketing Authorization Holders (MAHs) across pharmacovigilance, including the risk management system, are lacking. Furthermore, little is presented on the impact of patient review of additional risk minimization measures materials. We present a tested Pharmacovigilance Patient Centricity Framework describing key focus areas that can create the necessary infrastructure for systematic PE in effective risk minimization materials. Implementation of this framework highlighted the importance of collaboration to drive PE across the company at both local and global level, and externally, as relationships are established with patient organizations and best practices are shared with other MAHs. Therefore, this framework can be considered by other companies as a basis for developing a patient-centric approach to integrate the patient's voice into pharmacovigilance deliverables.

Indexed as

Patient ParticipationPharmacovigilanceDrug-Related Side Effects and Adverse ReactionsHumansRisk ManagementFrameworkPatient centricityPatient engagementPharmacovigilanceRisk minimization

Identifiers

PMID40715747
PMCPMC12579661

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Registered trials

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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.