08.29.25 -- Make Your Clinical Trial Process More Efficient With Software And Services

Our consultants are experts ready to formulate data strategies to guarantee consistent data integrity. We ensure that your study remains inspection-ready at every stage of development.

IQVIA One Home for Sites is a platform that serves as a neutral aggregator, connector, and communicator of the key systems and tasks a clinical research site needs to perform across all its trials.

Medable AI has the potential to alter how clinical trial software is built and deployed. By making the build process more efficient and innovative, bring life-saving treatments to market faster.

Computer System Validation to cover all your GMP, GLP, GCP, and QA/QC software applications. CompliancePath currently has 30+ active projects globally supporting clients in CSV/CSA compliance.

Florence’s eTMF boosts quality and accelerates start-up across all of your studies. Quickly configure your eTMF with intuitive workflows, flexible access controls, and powerful document tools.

Medidata offers out-of-the-box integration across #1 EDC, CTMS, and eTMF. Automation across data capture, document workflows, and reporting enables faster trial setup and execution.

Revolutionize design with IQVIA eCOA Sculptor’s intuitive drag-and-drop interface, real-time feedback integration, and live simulations—streamlining UAT, updates, and protocol amendments.

Revolutionize your approach to clinical trials at DPHARM: Disruptive Innovations to Modernize Clinical Research, taking place September 16–17, 2025, in Philadelphia. This conference showcases cutting-edge strategies and technologies designed to reduce patient and site burden, streamline operations, improve data quality, and accelerate access to therapies. Register now