Amencefs - Cro

We provide Clinical Data Management & EDC & SAS Programming services for clinical trials. We are an Accredited Partner with Medidata, and use Medidata RAVE EDC We also use VieDoc EDC, DATATRAK EDC, and ClinCapture Captivate EDC. 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 more than 18 years. Our service also includes Rescue Studies, Migrations, 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 attest to the speed at which we deliver work and more importantly the quality of our work. The Phase I-IV clinical trials we support get the attention they deserve from our experts in the area. We are flexible in partnerships (with sponsors and CROs). Think of Amencefs as an extension of your team. We pride ourselves on delivering high-quality service with flexibility and responsiveness. – Agbessi Gblokpor, President & Executive Director of Operations