The Art Of Accelerated Study Closeout: End Of Study Solutions

The transition to fully digitalizing study files after a trial represents a transformative shift in processes offers substantial advantages. With the widespread adoption of decentralized trial models, ensuring remote compliance oversight has become paramount, rendering traditional document-centric end-of-study procedures obsolete. In today's fast-paced development environment, the need for accelerated cycle times and continuous audit readiness is indisputable.

Discover how eClinical Solutions has excelled in streamlining the study closeout process using Medidata's Site Cloud: End of Study solution. They have not only expedited their study closeout procedures but have also effectively managed the increasing complexity of clinical trials.

During this session, Grant Williamson, Sr. Director, Clinical Programming of eClinical Solutions and Pat Pollard, Solution Services Principal of RCM at Medidata delve into the following key areas:

1. Common challenges in the end-of-study process.
2. The impact of transitioning from manual media distribution and management to electronic methods.
3. How the alignment of technology, people, and processes streamlines the study closeout, creating value for sponsors.
4. The advantages of leveraging a digital platform for the digitization and sharing of all end-of-study data.

Gain valuable insights from eClinical Solutions regarding their implementation approach and the remarkable results they have achieved in clinical trials by watching the full video below.