Data management is an indispensable part of clinical trial projects, and accurate and standardized data is crucial for subsequent data analysis and summary. We have built an information system in line with GXP, 21CFR part 11 specifications, and established a standardized data management process, committed to providing customers with accurate and high-quality data management solutions.
Compliance with GXP specifications, providing quality-assured data management throughout the clinical trial lifecycle and beyond
Nearly 90% of the data in clinical trials comes from the central lab, and the assurance of data quality not only affects the seamless operation of the project, but also directly impacts future NDA/BLA filings/application.
Since our founding, KingMylab has understood the importance of accurate, reliable, and traceable laboratory data. We provide timely, on-demand online data reporting and cross-checking with clinical center or third-party data systems. We also support up to 15 years of free data preservation services to ensure that your project data meets the requirements of registration.
Customized project report data
Professional DM team and IT team capable of develoingp project data reports based on project requirements
Efficient data interaction
Direct transmission of multiparameter data with clinical centers or third parties to ensure real-time online access to project data
Standardized data preservation and migration
Rigorous data management process and complete data migration plan to safeguard data integrity, security and stability
Comprehensive protection of data security
Advanced server configuration and network security settings ensure data storage, transmission, usage, and sharing security