• In today’s fast changing world, many a times it becomes imperative to migrate clinical legacy data to the requisite format as per FDA guidelines (FDA Study Data Specifications). Our services can be customized to transfer any form of data in an efficient and time saving way.
• We at QED use Clinical DI, a high end tool from SAS to convert any form of legacy data to CDISC compliant SDTM formats. This helps us do away with the conventional way of transfer using the data entry personnel. We can get your new database system up and running in considerably less time and with less conversion effort. Working with the data directly helps eliminate majority of human error.

 

Associated CDISC Member

We at QED Pharma:

• Have the complete Data Sciences Team trained in SAS Clinical DI by reputed trainers from SAS Institute
• Work with the latest version of SAS Clinical DI Studio (version 4.21)
• Have the competency to handle any form of legacy data
• Proficiency in handling globally recognized CDISC SDTM standards

 

Data Management
Biostatistics
SAS Programming