Medical Writing Clinical Trial Transparency and Disclosure Publisher perspectives on plain language summaries of scientific publications: An Open Pharma survey
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Volume 33, Issue 3 - Clinical Trial Transparency and Disclosure

Publisher perspectives on plain language summaries of scientific publications: An Open Pharma survey

Abstract

Plain language summaries (PLS) of scientific publications can help to make scientific literature more understandable. In healthcare, PLS can contribute to informed decision- making by healthcare professionals, patients, and their caregivers. In late 2022 and early 2023, the multi-sponsor collaboration Open Pharma developed a 16-question survey to collect the perspectives of journal editors and publishers on PLS and whether they align with the Open Pharma PLS recommendations. A total of 29 surveys were completed, representing 26 individual journals and seven publisher portfolios. Of these, 19 journals and two portfolios did not offer PLS as an option to authors, and one portfolio respondent was unsure. The survey showed variability in format, location, and peer review practices for PLS, and inconsistent tagging of PLS for PubMed indexing. The results highlight the need for more journals to accept PLS and follow best practice recommendations to ensure PLS are peer reviewed and discoverable.

Medical Writing. 2024;33(3):54–61. https://doi.org/10.56012/pzwh6593

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Articles

Clinical trial transparency and disclosure from the medical writing perspective
From the Editor
President’s Message
EMWA News
Protection of personal data and commercially confidential information under the Clinical Trials Regulation (EU) No. 536/ 2014 – EMA “Revised CTIS Transparency Rules"
Making the leap: Transparency requirements for clinical trials moving from one regulatory framework to another
Navigating the complex landscape of clinical trial transparency: What medical writers need to know
Plain language summaries of clinical trial results: What is their role, and should patients and AI be involved?
The 2023 CORE Reference Utility Survey: Perceptions on a best practice tool for globally applicable clinical study reporting and provision of continuing professional development resources for the regulatory medical writing community
Creating educational materials about clinical research data for patients and the public: A multifaceted journey in the current digital age
Publisher perspectives on plain language summaries of scientific publications: An Open Pharma survey
Medical writing in Italy in 2024: Results of the first Italian business and compensation survey
News from the EMA
Digital Communication
Medical Communications and Writing for Patients
Regulatory Public Disclosure
In the Bookstores
Publications
The Crofter: Sustainable Communications
Good Writing Practice

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Raquel Billiones

Co-Editors

Evguenia Alechine

Jonathan Pitt

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Victoria White

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Alicia Brooks Waltman

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Anuradha Alahari

Jennifer Bell

Nicole Bezuidenhout

Claire Chang

Barbara Grossman

Sarah Milner

John Plant

Sampoorna Rappaz

Amy Whereat

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Nicole Bezuidenhout 

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Somsuvro Basu

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Adriana Rocha

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Ana Sofia Correia 

Gained in Translation

Ivana Turek

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Wendy Kingdom / Amy Whereat

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Pablo Izquierdo / Alison McIntosh 

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Maria Kołtowska-Häggström

Lingua Franca and Beyond

Maddy Dyer

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Lisa Chamberlain-James

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Payal Bhatia

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Evguenia Alechine

My First Medical Writing

Anuradha Alahari

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Tiziana von Bruchhausen

Pharmacovigilance

Clare ChangZuo Yen Lee 

Regulatory Matters

Sam Hamilton

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Louisa Ludwig-Begall / Sarah Kabani

The Crofter: Sustainable Communications

Jeff Blair / Luiza Ventura

Veterinary Writing

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Elise Langdon-Neuner

Phil Leventhal

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Chris Monk