Explore how ArisGlobal enables life sciences organizations to plan, track and control all activities related to the set-up, conduct, and closeout of clinical trials using a simple, intuitive interface.

Explore how CTMS capabilities can help uncover hidden study risks with industry-standard questions in the CTMS library, score study risk based on likelihood, impact, and detectability, and manage key risk indicators.

While clinical trial innovations result in increasingly diverse data sources and study types, discover why this diversity also brings additional concern about patient safety and data quality.

LifeSphere electronic Trial Master File (eTMF) system streamlines inspections, ensures compliance readiness, and improves efficiency from study start to close-out.

With ArisGlobal’s LifeSphere Clinical Trial Management System (CTMS), learn how you can meet study timelines and reduce stress in a single unified platform.

This eBook examines the rising trend in compliance findings due to incomplete or poor-quality Trial Master File (TMF) submissions.

An eTMF system can help Clinical Operations professionals manage the deluge of documents and data, but what capabilities are right for your situation? What is the best way to make the move to a modern eTMF from paper, spreadsheet trackers, or legacy tech to a new eTMF? Hear answers to these questions and more from a fellow Clinical Operations leader with experience in making the transition to an eTMF built for today's research ecosystems.

LifeSphere electronic Trial Master File (eTMF) is an easy to use application that streamlines inspections, future-proofs compliance and saves time and effort for all key stakeholders, from study start-up through closeout. 

Legacy electronic Trial Master File (eTMF) systems are built on proprietary data standards or old file sharing tech. ArisGlobal is forging a new path.

Biocon is India’s largest biopharmaceutical company and an early adopter of the LifeSphere eTMF system. Rashika Suri, Head of Clinical Quality and Compliance at Biocon, discusses the importance of collaboration when implementing new technology.

In this case study, gain insight into how a large CRO overcame the struggle to meet the service requirements of clients in a cost-effective and efficient way.

Discover how a leading global pharmaceutical company solved the problem of managed the distribution of safety reports by their clinical operations team.

This webinar discusses current operation models in the world of Safety Document Distribution and the modern approaches to reduce complexity and compliance risk, as well as increase efficiency.

Technology can help automate much of the safety document distribution processes. Learn why it’s prudent to explore the reasons why it makes sense for organizations to move to an automated system.