LAVIS Team brings to bear a unique constellation of expertise in clinical research, technology, and business intelligence and analytics to deliver meaningful solutions.

Study Builds
  • Develop eCRFs and Data Validation constraints using edit checks and custom functions in support of clinical studies
  • Create eCRF data entry screens based on approved CRF casebook
  • Implement system edits in data entry screens
  • Utilize validation procedures as needed for clinical studies
  • Build edit checks and custom functions to enforce data validations

Custom Reports Development
  • Develop custom reports based on your specific requirements in different functional areas including protocols, subjects, reviews, financials, EDC, etc.
  • Implement solutions using technologies such as SSRS, Jasper Reports, etc. based on the Clinical Research Systems in use at your research institution
  • We work with your internal subject matter experts to understand the reporting requirements in detail, and develop, test, and deploy the reports in your systems

Data Migration
  • Migrate data from your existing systems into your target systems
  • We have significant experience managing clinical research data migration projects as well as the actual migration of data into different systems including CTMS, IRB, EDC systems
  • We have expertise in all database technologies such as Oracle, MS SQL Server, and MS Access, etc.

Technology Expertise
  • Provide clinical research technology expertise for research organizations including research institutions, pharma, biotech, CRO, SMO and ISNs
  • Technology support for business development needs at small to medium pharma, biotech, SMO and ISNs
  • Provide data analytics support for study feasibility and clinical data management including data analysis, database design, data audit, and data extraction