Bright’s Data Management staff have ten or more years’ experience and provide CDISC compliant data at no extra cost. Whether your trial uses paper case report forms or runs on our electronic data capture platform, our international trial experience brings a depth of knowledge that even a small single site study benefits from.
Your secure access through our 24/7/365 portal puts you in the command center able to make operational decisions on the fly and save time and money, reduce or increase monitoring visits and respond to alerts and red flags immediately no matter where your sites are.
Our standard of frequent communication starts early with your entire team, regardless of whether it’s a multi-national group of players from several vendors or just one person. We’re flexible, responsive and proactive.
We provide the standard double data entry as well as both electronic and manual review of data, all the while performing frequent data trend observations.
Bright can provide E-randomization on our Oracle-based platform. Your data will be 21 CFR part 11 compliant.
We also provide site and overall real time drug accountability reports and can deliver your database fully developed within 6-12 weeks after case report forms are finalized.