CASE STUDY


Producing a series of related Phase III clinical study reports for a submission


CLIENT NEED

A large number of Phase III CSRs with overlapping timelines required authoring with condensed timelines. Insufficient in-house resource was available.

OUR SOLUTION

Key senior writers completed training on client guidelines and procedures. One key writer was assigned to be the main contact for the project to manage the overall report-writing process. Additional writers were assigned to provide quality control and assist with document preparation.

OUTCOME

A consistent, accurate series of reports were produced within the strict timelines. Further work was assigned.

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