Our primary goal in data management is to provide a high-quality, cost-effective solutions compliant with the most rigorous regulatory standards. Our team focus on the development and maintenance of databases for a range of study types, from Phase I – IV and post-marketing clinical trials. We strive to provide clean data using industry standard tools and formats, on time and to budget.
We customise our offerings based on your requirements for electronic data capture (EDC) or eCRFs, and/or paper CRFs using globally acceptable fully validated 21 CFR part 11 compliant systems for data management. We leverage industry-leading technologies to provide the most efficient solutions for your study.
Our clinical trials DM services include: