Abstract
From scurvy to Covid-19: The role of clinical trials, and medical writing’s crucial role in the process
The medical writing community is intrinsically involved in regulatory documentation that spans the entire timeline of clinical research – from study protocols and informed consent to clinical study reports and even post-market pharmacovigilance. “Clinical Trials” is therefore an appropriate theme for an issue of Medical Writing.
Medical Writing. 2023;32(1)6. https://doi.org/10.56012/eoag8863
Download the full article
Visit the EMWA website
Search
Articles
Links
Editoral Board
Editor-in-Chief
Co-Editors
Managing Editor
Victoria White
Deputy Managing Editor
Alicia Brooks Waltman
Associate Editors
Section Editors
AI/Automation
Biotechnology
Digital Communication
EMWA News
Freelancing
Gained in Translation
Getting Your Foot in the Door
Good Writing Practice
Pablo Izquierdo / Alison McIntosh
In the Bookstores
Publications
Medical Communications/Writing for Patients
Medical Devices
My First Medical Writing
News from the EMA
Pharmacovigilance
Regulatory Matters
Regulatory Public Disclosure
Louisa Ludwig-Begall / Sarah Kabani
The Crofter: Sustainable Communications
Veterinary Writing
Editors Emeritus
Layout Designer
Chris Monk