New Guide Explains Role of Regulatory Medical Writers

Regulatory writing is a specialist type of writing that supports the drug approval and development process. The role of the regulatory writer is to prepare the scientific documents that pharmaceutical companies need during the development of a drug. As such, regulatory writers play an important role in bringing new drugs to market and improving patient care. Access the full guide here.

(Source; Dr. Deborah Brix, A writer’s role in Drug Development, Burntsky Ltd. Publishing)