December 4, 2019
While data is at the center of every research project, data management strategy and implementation can seem mysterious. Data management is more than just issuing queries and locking case report forms – it includes all the steps and systems that you’ll need to prevent user error, flag problems for rapid response, and prepare datasets for analysis. In rare disease trials, data management is essential to utilize every data point from a limited number of participants.
TRiNDS Data Management offers comprehensive and customized data management services to neuromuscular rare disease trials. A lead data manager first helps you choose the right systems and processes for your specific project. The data manager will create case report forms, electronic data capture systems, automatic validation processes, quality control, and data imports and exports. Our data management team leverages their extensive experience and training to help you plan for the data expected for your patient population.
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.
