Let us help you with your clinical trial data.
Expert consulting services
Who We Are
Our Vision
Our vision is to be a leading clinical data management consulting firm in the clinical trial industry by providing innovative solutions excellent service to our clients.
Clinical Data Management
14+ years of experience in Biotechnology, Medical Device, Pharmaceuticals, Diagnostic studies, Covid, Oncology, Women's health, Transplant, Bio-banks, Endocrinology, Regenerative medicine, Flu, Cell-free DNA, Cardiology, pediatric/adult studies and Phase I-IV studies.
Clinical Data Management Document Creation
We can provide customized standard operating procedures (SOPs) or manual of procedures (MOPs), work instructions (WIs), data management plans (DMPs), data review plans (DRPs), free text review plans (FTRPs), and offer improvement solutions that will help you get organized, compliant and auditable.
Data Review & Data Cleaning
Experience in Medrio, REDCap Cloud, Clincapture, Merative Zelta, Simplified Clinical, DSG and TrialKit.
EDC System Training Aids
Expertise in creating PowerPoint presentations for EDC training, CRF Completion Guidelines (CCGs), hand-out instructions for Monitoring and PI sign-off.
Electronic Data Capture (EDC)
Expertise with the following EDC systems: Medrio, Clincapture, Merative Zelta and Simplified Clinical.
Study Oversight
Experienced working with clinical research organizations (CROs) and academic research organizations (AROs). Lab reconciliation and data transfers.
Paper Case Report Forms (CRFs)
If you have a study that needs paper CRFs, we can create them for you. We can also print them in 3-part NCR copies and ship them to you right away!