Jun 9, 2025 · b. Data Collection: Collect data from study participants using electronic or paper case report forms (CRFs) or electronic data capture (EDC) systems required by the sponsor of …

IDDI is the center of excellence in regulatory statistics and clinical data science with deep expertise in handling complex data challenges from Pre-IND through to regulatory submission.

Keeping the coverage practical, the author focuses on the most critical information that impacts clinical trial conduct, providing a full end-to-end overview for clinical data managers.

Clinical Data Management (CDM) is a vital component of clinical research, responsible for producing high-quality, reliable, and statistically sound data from clinical trials.

This SOP applies to all personnel involved in the management of data for clinical research conducted through the Clinical Trials Office. This SOP oversees set up, access, management …

This special issue on the Practice of Clinical Data Management Worldwide offers four insightful perspectives on the evolution and practice of CDM/S in four very different regions of the world.

Advancements in technology are revolutionizing Clinical Data Management. Several innovations are changing how we collect, analyze, and report data in clinical trials: