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CRO

Contract Research Organization

We work with pharma/biotech/device companies to organize and implement their studies. The CRO is the logistics middleman that takes care of all the operations of a clinical study from start to finish, and delivers the data to the pharma company. 

Study Start Up
  • Protocol Design
  • Site Selection
  • Regulatory Strategy
  • IRB Submission
  • CRF Creation
  • Database Setup
Subject Enrollment
  • Randomization
  • Site Management
  • Site Training
  • Clinical Monitoring
  • Tracking Data & Queries
  • Biological Sample Tracking
Study Close Out
  • Database Lock
  • Data Cleaning
  • Final Analysis
  • CSR Compilation
  • Regulatory Submissions
  • Publication Support
Medical Services
  • Clinical Trial Rescue Services
  • Audit & Inspection Preparation
  • Independent Data Monitoring