eTMF Solutions

1. Automation Solutions For Clinical Operations And Data Management 5/27/2022

   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.

2. Industry-First eTMF AI Reduces Risk Of Document Misfiles And Metadata Errors 4/6/2023

   PhlexTMF offers the industry’s only next-generation eTMF AI, providing expert suggestions at the critical document upload step, reducing errors, and improving TMF quality, completeness, and timeliness.

3. How LifeSphere eTMF Extends Clinical Collaboration 3/7/2022

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

4. Accelerate Study Startup Through Better Collaboration 3/3/2025

   With 80% of trials failing to enroll patients on time, improved collaboration between sites and sponsors is essential.

5. Your Early "Warning System" To Assess Risks To TMF Health 4/19/2022

   Introducing the TMF Health Score – an expert methodology that provides an “early warning system” to commonly overlooked issues that often lead to inspection findings.

6. TrialKit eTMF 8/8/2024

   Manage inspection-ready clinical trial documents with confidence for faster study execution with TrialKit’s electronic trial master file system.

7. Phlexglobal Experts Fill The Gaps In eTMF Management 12/16/2022

   Enable busy study teams to assess, prevent, and manage risk across the entire TMF spectrum – improving inspection-readiness with less effort.

8. An eArchive That Is Always Inspection Ready 10/30/2023

   Meeting regulatory requirements for storing documentation for 25+ years, review this clinical trial data retention solution's comprehensive set of features.

9. Improve eTMF Document Processing Speed And Quality

   In any eTMF — at any stage — ensure timely, right-first-time processing from source to archive with help from Phlexglobal leadership in TMF best practices.

10. Your Author-To-Archive Platform For Regulated Content 6/30/2022

    Discover how to create, edit, review, finalize, translate, submit, and archive your clinical trial documentation all within one single platform.