We engineer applications to secure and restructure clinical databases. We reorganize and conform your clinical datasets against CDISC/regulatory standards.
Execute real-time exploration of millions of clinical data records. Forget tedious programming tasks. Just let your team walk securely onto your datasets/database.
Deliver robust and comprehensive publication-ready clinical reports. Yes, you can do that easily, securely and efficiently. We have the expertise and the solutions.
Do you have vast amounts of heterogeneous trials and legacy data stored in your databases and/or clinical data management systems?
Extracting relevant information can become a tedious task, especially in therapeutic areas where clinical data records are complex and difficult to report and/or to analyze securely.
Creating innovative tools and CDISC compliant services to easily manage large amounts of clinical datasets is the core expertise of AdClin.
AdClin provides a unique expertise in SDTM / ADaM standards, from the delivery of error-free submission-ready packages, to the conversion and pooling of legacy databases, and offers consulting to help you matching the CDISC® and FDA's requirements.
AdClin is one of the most seasoned experts in CDISC Controlled Terminology. We provide a range of services to help you navigate efficiently values and definitions, and streamline the process of implementing them into your SDTM workflow.
AdClin has created new generation software tools maximizing the efficiency and security of clinical data reporting: by easily and securely navigate datasets, produce any kind of tables and listings, and automatically generate state of the art clinical reports.