CTMS Featured Articles

1. What Sites Wish Tech Vendors (And Sponsors) Heard At SCDM But Probably Didn't 10/8/2025

   During a Society for Clinical Data Management (SCDM) panel discussion, three site-side representatives discussed the challenges clinical research coordinators have executing their clinical duties amid increasingly complex data entry demands.

2. SCDM 2025: Practical Advice From Global Regulators — Including The FDA 10/6/2025

   Discover what regulators from around the world, including the FDA, think should be top of mind for clinical data managers.

3. Is Double Programming Really Required For Validation? 3/10/2025

   Double programming has been the gold standard for validation, but technological advancements and improved sponsor oversight of CRO deliverables have introduced more efficient and reliable alternatives.

4. Why We Need Technology Consolidation In Clinical Trials 8/16/2024

   As more and more trial designs incorporate technologies that generate an immense amount of data, data managers struggle to continuously interconnect disparate systems and standardize data. All of this fuels the need for technology consolidation.