All clinical investigations begin with the development of a clinical study protocol written by a multidisciplinary team and coordinated by the medical writer. Lean regulatory writing processes and tools help streamline complex document development, including protocols or other submissions to regulatory authorities and ethics committees.
In this whitepaper, we explore how these valuable tools, including software, templates and collaborative work processes, can provide practical solutions to common challenges medical writers face.
Topics include:
Using innovative tools and lean writing processes to accelerate regulatory document writing