DATA ANALYSIS AND REPORTING
The management of data produced by clinical trials is a task that requires efficiency, expertise and the ability to deliver on time without compromising quality and integrity. SGS is a world leader in data analysis and reporting. Our biometrics team – the largest independent data management team in Europe, staffed by over 140 data experts – has over 15 years of experience using the latest methods to meet the data management, biostatistics and medical writing needs of a wide range of clients.
Our services are flexible enough to be shaped into a tailored clinical trial data management program to meet your particular needs, whether they be for a stand-alone project or a full drug development program. Our world-class, comprehensive services include:
- Database design and setup – We create and manage a database to your specificatons, design CRFs and can write the clinical trial protocol
- Electronic data capture (EDC) – We have vast experience in setting up eCRF applications using cutting-edge solutions and managing EDC data
- CDISC compliance – SGS is an Advisory Board member for CDISC, and as a registered provider we have converted over 140 legacy trials into the CDISC model and submitted successful e-submissions in CDISC for many clients
- Statistics consultancy – We can provide advice on sample size calculations, randomization, and DSMB services
- Report writing – Our multilingual writers produce a wide range of clear, professional products to communicate your findings. Our clinical research reports adhere to ICH-E3 guidelines