Volume 33, Issue 3 - Clinical Trial Transparency and Disclosure
Regulatory Public Disclosure
Author: Sam Hamilton
Abstract
Section Editor and Author: Sam Hamilton
Medical Writing. 2024;33(3):95–100. https://doi.org/10.56012/vhdv1639
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Clinical trial transparency and disclosure from the medical writing perspective
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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
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