Services - Overview
Experienced Team to support your clinical trials
Data Management, SAE Management, Biostatistics, and
Reporting have been the cornerstones of SCiAN's business since
1986. With a portfolio of over 650 studies, SCiAN's
dedicated teams can step in and support all:
- Study design and protocol development
- Data management our CDMS systems
offers both paper-based and EDC solutions
- Medical monitoring, drug safety / SAE management
- Biostatistics: all phase I, II and III designs, including
traditional
- Medical writing (protocol development, CSR writing,
manuscript prepration)
aspects of a study. All SCiAN personnel are trained in CDMmanager (our
paper based CDMS system) and EDCPRO and
SAEPRO making the transition seamless for your
study, in oncology or other
indications.
Studies completed by SCiAN ranged from small and complex
phase II oncology trials to large-scale global II/III trials
managed in collaboration with the Sponsor's team and
clinical / site management CROs.
We offer a comprehensive set of data management
services to:
- Launch your study (study design, protocol writing, CRF design,
database build, testing, site training, etc.)
- Monitor and update the database design to match
actual usage by Study Coordinators, Monitors and Data
Managers
- Perform Medical Monitoring, SAE management
- Perform central data monitoring to complement site monitoring /
SDV
- Manage DSMBs
- Prepare for interim locks and database exports
- Manage data uploads / imports, coding, SAE reconciliation
- Prepare for final database lock, audit, release and
archival
- Generate SAP, TLFs, CSRs.