A top-10 global pharma company needed to produce a large number of Clinical Study Reports (CSRs) for a range of globally, regionally and locally sponsored trials. The client needed a solution to cost-effectively produce these documents within a defined time frame, recognising that the completeness and quality of source data was highly variable. The objective is to provide high quality and efficient authoring of CSRs and associated web postings.

A coordinated program with a blended onshore offshore model is followed for the service delivery. Editorial, QC and client liaison support is provided onshore. Consultancy is provided to the client on the appropriate CSR type. The majority of service delivery effort is based offshore, generating significant cost advantages.

The project is still ongoing.