Kathleen LeGrow
Articles
Integrating CMC Document Preparation into the Development Process for Vaccine INDs
Rachel Thornton;Anna Hagen;Robert Sitrin;Tracy Janus;Kathleen LeGrow;Laura Howson;Anne Aunins;Robin Robinett
September 1st 2003Vaccine process development is complex, and so are the documents required before clinical trials begin. Technical writers and editors can effectively coordinate the timely authoring, reviewing, and auditing of regulatory documents, minimizing filing delays.
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