SCL IT Technologies

SAS Programming

We provide SAS programming services for the pharmaceutical industry in support of statistical analysis and data management activities. When you work with us, you can be as hands-off or as hands-on as you want to be. For example, you can provide just the study protocol, SAP, data and CRFs, and we’ll deliver validated output. Or, you can provide us very detailed specifications and perform the validation in-house. Whatever your clinical trial programming needs, Our staff have the skills, efficiencies, and experience to produce high-quality, accurate, on-time deliverables .
SCL IT Technologies biostatisticians and statistical programmers provide comprehensive biostatistics and statistical programming services to support clinical, pre-clinical and patient reported outcomes for pharmaceutical, medical devices and biotech companies.

Biostatistics services include:
  • Trial design and protocol development
  • Sample size calculation/justification
  • Randomization schemes
  • Statistical analysis plan (SAP) for different phases of clinical studies
  • SAP for Integrated safety and effectiveness (ISS/ISE)
  • SAP for briefing documents to regulatory agencies and publications
  • Data Monitoring Committee/independent statistician services
Statistical programming services include:
  • Data conversion
  • Statistical Tables, Figures, and Listings
  • CRF Tabulations and Patient Profiles
  • Data Management Listings (e.g., QC Listings)
  • Edit Checks
  • General Dataset Remapping/Restructuring
  • SAS programming tailored to individual Sponsor’s needs
  • CDISC-compliant and submission-ready datasets and documents
  • Statistical tables, listings, and figures for clinical study reports
  • Pharmacokinetic and pharmacodynamic analyses dataset preparation
  • CRF Annotations as per SDTMIG
  • SDTM and ADaM development as per C-DISC standards
  • Performing Edit checks and Data cleaning
  • Validation through validated procedures
  • Well experienced programmers for ISS/ISE
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