The role of medical writing in clinical research

Abstract

Medical writing is a specialized field that involves the creation of scientific documents by writers with a detailed understanding of medical and scientific concepts. In the past few decades, medical writing has seen substantial growth in India. This field encompasses the creation of regulatory documents, safety reports, publications, and educational and communication materials pertaining to health and healthcare products. These documents are crucial in various aspects of healthcare, including clinical research, regulatory affairs, marketing, and education. Medical writing plays a crucial role in the successful execution and documentation of clinical trials. This article delves into the responsibilities of medical writers, the importance of their work in the clinical trial process, and how they ensure regulatory compliance and clear communication of clinical trial outcomes.