May 26, 2021
TRiNDS Data Management Services
Every clinical trial relies on data to answer scientific questions. Rare disease clinical trials are designed to answer questions with smaller sample sizes of hard-to-find participants. Every day point matters – one missing measurement can make the difference in whether a trial can answer its questions. Data from rare disease populations can be harder 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 full-service data management support including our regulatory compliant electronic data capture (EDC) systems. Every project is assigned a Data Manager who leads the data management support of each project. 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. Our team can provide everything from case report form design, database design and development, database user acceptance testing (UAT) and validation, 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.
