With more than 20 years of experience in the development of clinical trials, the MHICC has built a dedicated and highly competent team of clinical programmers committed to provide full-service support to enable life sciences companies and researchers to innovate with confidence, maximize opportunities, and, ultimately, drive human health outcomes forward.

MHICC’s Electronic Data Capture (EDC) System

The web-based data management system, InForm® EDC, provides a centralized location for the study team to review real-time case report form (CRF) data. The system allows for the secure and accurate collection and cleaning of the data from each study. This comprehensive tool, developed by Oracle, provides functionality in the areas of study design, data entry, data clean-up, coding of terms with MedDRA and WHODrug, source data verification, email alerts, Data review, complex and ad-hoc reporting with Cognos®, real-time web access, audit trail, and export of the clinical data for analysis purposes.

MHICC, Platinum CDISC member (SDTM, ADaM, Define-XML)

Our deep and comprehensive understanding of CDISC standards, which stems in part from our participation in international clinical trials, ensures efficient and accurate CDISC services in terms of Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) programming including Define-XML and Clinical Study Data Reviewer Guide (cSDRG). We support CDISC requirements for all clinical trials.