11.09.23 -- How To Accelerate Digital Clinical Transformation Through A Holistic Approach

Numerous aspects of oncology clinical research present inherent complexities. Explore how advanced technology solutions have the potential to simplify the operational aspects of oncology trials.

Examine the three reasons why simplifying your clinical data flow can increase operational oversight, shorten data management cycle times, and reduce the manual burdens on data management teams.

See how Bellerophon Therapeutics, a clinical-stage biotherapeutics company, was able to save its clinical development program through the use of objective, continuous digital outcome measures.

Watch as presenters from Medidata dive into the most common roadblocks customers face when adopting a modern clinical trial management system — and how to avoid them.

Discover an integrated eSource/EDC model, in which source data is collected electronically and then transmitted automatically, allowing sponsors to review, query, code, lock, and extract the data.

Consider how the orchestration of integrated response technologies for randomization and trial supply management and electronic clinical outcomes assessments can improve studies.

Director of Partners and Alliance Management at HealthVerity KC Ahlberg discusses key trends related to the use of RWD in clinical trials and the value sponsors are realizing through data linkage.

EU Annex 11 outlines the European Union’s regulations for using computerized systems during trials. Uncover why sponsors and sites needing approval for new medical treatments, must follow Annex 11.

Each decentralized trial is unique and has its own set of requirements. Based on a trial’s design, consider how to plan for necessary system interactions, leverage the data collected, and select the right partner.

Take these steps when repositioning your clinical data management team to unify cross-functional reviews and align processes and technology to meet the demands of digital trials.