Clinical Programming

Clinical trials have complex computational needs. The correct programming approach to deal with such needs involves a robust technology-based trial ecosystem. Strategically designed and programmed technology solutions are the key to successful clinical programming.

At Centreum we offer you a comprehensive range of high quality and cost-effective clinical programming services. We offer accurate data analysis in compliance with regulatory requirements while always being able to adjust to the business needs. We have vast experience in designing, analyzing and reporting clinical studies across a broad range of therapeutic areas that are supported by robust processes and global infrastructure.

Statistical Analysis & Programming
  • CDISC Subject Matter Experts
  • Statistical analysis datasets according to SAP
  • A dynamic template-based reporting system for creating Tables, Figures and Listings
  • Statistical reports
  • Modular programming method
  • Generic validated macros
  • Standard QC Process

Clinical Database Programming
  • Setup and define the database
  • Central data implementation (such as laboratory data, central ECG readings etc.)
  • Validation checks and queries according to the data validation plan
  • Centralized global macro library
  • Data listings, patient profiles, summary tables and figures
  • Clinical Study Reports and Publications

System and Quality Management & Administration
  • Structured Organization –Charts, position descriptions, roles and responsibilities
  • Continuous Improvement Framework
  • Training Management Systems, selection and implementation
  • Coordinate help desk requests and ensure compliance with service level agreements
  • Create proactive or reactive regulatory strategies to respond to anticipated or unforeseen regulatory hurdles
  • Continuous administrative and technical support for all clinical information systems
  • Evaluate and Implement clinical information systems and data management platforms (EDC, CTMS, eTMF, eDiaries, payments systems, electronic regulatory filings etc.)