We specialise in clinical trials.
MCS resources have experience throughout the clinical data management process.
Starting with definition and review of the study protocol and Case Report Forms, through data management planning to ongoing data review and preparation for analysis, we can help guide your study through the data management lifecycle.
We know trials systems.
MCS are proficient in the selection, implementation, upgrade and operation of clinical trials systems. We have worked with many different systems including OpenClinica, InForm, REDCap, Webspirit, Oracle Clinical, and Clintrial, plus other commercial systems and some bespoke software systems for randomisation, drug/kit management, and general trial management.
We are not "hard core programmers"; we are applications experts.
We've done it before.
MCS are skilled in managing multiple concurrent study system implementations (eCRF and paper based). System and study validation, documentation and training are key capabilities. We advocate the definition and revision of SOPs, standards and templates to facilitate efficient, high quality data collection and data management.