Regulatory Writing
Regulatory medical writing produces a variety of clinical documents across the treatment life cycle, from summarizing and writing data from clinical studies to generating regulatory suggestion documents. After the treatment has been approved by the regulatory authority, post-approval reports on the treatment of patients are generated. Clinical Study Reports (CSR), the Common Technical Document (CTD), and other clinical documents created by medical writing services using regulatory writing services are only a few examples of clinical documents generated by medical writing services utilizing regulatory writing services.
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