If you want to read about one of our project cases that deals about data conversion, then use the button below. 

We don't work for our clients, but side-by-side with our clients!

OCS Life Sciences has a specialised team for the conversion of clinical trial data for regulatory submissions. 

Equipped with innovative software our scientifically educated data managers and clinical programmers relieve you from the burden, allowing you to focus on all other aspects of your submissions.

Our services for data conversion include:
  • Project planning and management
  • SEND, SDTM and ADaM datasets
  • Define-XML for SDTM and ADaM
  • Study and Analysis Data Reviewer's Guides
  • Annotated Case Report Forms
Benefits from integration or pooling your data in CDISC-compliant datasets (without submission):
  • Publications on consolidates findings
  • Enhanced precision in efficacy analysis
  • Identification of rare safety signals
  • Better exploration of drug interactions
  • Starting point for ISS and ISE reports
  • Structured basis for data visualisation

Do you want to find out more about our Data Conversion services?

Or about Statistical Programming, Reporting & Biostatistics or our Mapping Engine?

Then get in touch with Melanie Schopp through the button below or at