We provide Data Management & EDC & SAS Programming service for clinical trials. We currently use Medidata RAVE EDC (Medidata Accredited Partner - https://www.medidata.com/en/company/amencefs-llc), VieDoc EDC, DATATRAK EDC, ClinCapture Captivate EDC, and Veeva. We specialize in study build, data management, protocol amendment changes, and Custom Function programming for multiple therapeutic areas including Oncology and medical device. We are a team of experienced Data Managers and EDC Programmers who have worked in the Clinical Research industry for many years. Our service includes Study Build, Data Management, Migrations, Custom Functions, System Integrations with IVRS systems, EDC URL setup with iMedidata and Cloud Administration, Core Configuration, Coder, Lab Administration, Safety Gateway, and Batch Uploader, setting up nightly SAS data extracts, programming extracts, aggregate checks, reconciliation and vendor reports, coding reports, and ad-hoc reports. Our specialization, streamlined process, and competitive cost set us apart. We provide services to Pharmaceutical companies, Biotech, Medical Device companies in North America and beyond. Our clients and sponsors love the speed at which we deliver work and more importantly the quality of our work. We deliver for our sponsors and were able to go live with forms in 4 weeks for a study originally built in another EDC system. Our work speaks for itself. So does our experience. The Phase I-IV clinical trials we support get the attention they deserve from our experts in the area.