Mr. John Redue

In Transisiton

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In Transisiton


John has more than 15 years of experience in the pharmaceutical/biotechnology industry as a regulatory medical writer. He has experience in preparing clinical R&D documents from the start of the IND to summary documents in the NDA/BLA. John has authored, managed, and overseen the document creation process, from inception to lifecycle management to electronic publishing and submission. He is currently the Communications Coordinator of the DIA MW Community.

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