At Prestige Scientific, we understand that data is gold in the clinical trial process. We work closely with our clients to understand their biometrics objectives such as writing protocols, study reports, responding to regulatory questions on statistics or study design, participation in upcoming regulatory meetings, or review of SAS data structures for CDISC-compliant ISS and ISE datasets. Your team may be responsible for clinical trial results being readily available in a common, easily browsible format to allow quick response to any untoward safety issues in ongoing or planned clinical trials and to permit rapid response to safety or efficacy queries by regulatory agencies.
We understand. We’d like to learn about your goals and objectives to see how we can provide the best solutions to drive your company forward.