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    Transitioning Between Medical Writing and Regulatory Affairs in a Contract Research Organization

    This article discusses transitioning from medical writing to regulatory affairs within a Contract Research Organization (CRO). Both roles are summarized and the similarities and differences between these two areas discussed. The author highlights why one might want to make the change in either direction and from her own transition experience, offers helpful hints for success. Introduction In the pharmaceutical industry, working in the regulatory field offers many possi...