The enhancement of effective data management strategies requires a thorough understanding of industry trends, technological innovations and the evolution of regulatory standards.
Over the last 15 years CROS NT has acquired extensive knowledge through the management of vast amounts of data generated by clinical trials. This strength enables CROS NT to improve speed, efficiency and cost effectiveness while conducting clinical trials, leading to flexible solutions for all phases of the drug development lifecycle. CROS NT is equally capable in performing data management activities with eCRF or paper CRF, alternatively customers can adopt one of its hybrid solutions according to their business needs.
To ensure the timely delivery and maximum quality and integrity of clinical data, CROS NT adheres to comprehensive SOPs, supported by a robust project management model.
All data management systems are 21 CFR part 11 compliant to provide a fully validated data management environment.
Our Data Management services include:
Since joining CROS NT in 2010, Monica has the responsibility of developing SOP and guidelines for data management activities including leading data-entry staff and assigning appropriate resources to a project. 
