Clinical Data & Document Solutions

Our ReadyClinical™ professionals utilize state-of-the-art, web-based, secure, clinical trial management, clinical data and document management software applications to execute and manage Phase I-IV clinical trials in a rapid and cost-efficient manner:

ReadyClinical™ CTMS client-centric clinical trial management system

ReadyClinical™ DOCS electronic trial master file for essential study documents

ReadyClinical™ EDC electronic data capture (eCRF electronic case report form)
paper CRFs are also available

ReadyClinical™ e-Vigilance – pharmacovigilance and SUSAR reporting

ReadyClinical™ e-CTD Generator – electronic CTD regulatory submissions (IND, IDE, NDA, BLA, PMA)