October 7, 2020
TRiNDS Data Management Services
Every clinical trial or research study collects data to answer scientific questions. How the data is collected, cleaned, and coded impacts its research utility. In rare disease studies, sample sizes are smaller, and each data point is critical. Data from rare disease populations can be hard to plan for – values that would be out of range in any other study will be expected in a rare disease study. You need expert data managers who understand rare diseases and can help you plan for your data from the beginning.
TRiNDS Data Management offers comprehensive and customized data management services to neuromuscular rare disease trials. Our team of in – house data managers leverage past experience in Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), Pompe Disease, and other neuromuscular disorders. Each project is assigned a data manager to lead the work – from case report form and database design, to electronic data capture systems, automatic validation processes, quality control, and data imports and exports. We partner with you to design the systems you need for high quality data.
TRiNDS offers expert data management services to sponsors conducting clinical trials throughout the development process. We customize services to each project to meet its unique needs. Contact us for more about how TRiNDS can help your project succeed.
