• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trials
    • Search Clinical Trials
    • Patient Notification System
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Clinical Trial Listings
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • Events
    • Newsletters
    • JobWatch
    • White Papers
    • Patient Education
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Trial Listings
  • Advertise
  • COVID-19
  • iConnect
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » EastHORN moves to Montrium's eTMF platform

EastHORN moves to Montrium's eTMF platform

October 3, 2017
CenterWatch Staff

Montrium, an industry provider of Electronic Trial Master File solutions, announced that EastHORN Clinical Services has selected eTMF Connect to optimize its clinical programs and TMF management. EastHORN, a European CRO, will implement Montrium's eTMF platform to increase transparency to enable greater collaboration with sponsors, improve compliance and provide greater value for its customers.

"We firmly believe that technology solutions will give us a competitive advantage in the crowded CRO market. The value a powerful eTMF solution could have on the advancement of our clinical projects and the increased transparency a centralized tool could have on collaboration with our partners were important considerations in deciding on the Montrium system," said Dr. Malgorzata Szerszeniewska, CEO of EastHORN Clinical Services. "It was also important that we selected an eTMF tool that not only supported us with a robust functionality set but was incredibly intuitive and easy to use. Montrium was a clear leader in its class, and Montrium's technical support with the implementation of the system in EastHORN has been exemplary."

Clinical organizations are now competing in a new world; where the pressures of clinical trials are more intense than ever. Whether it's to reduce trial timelines or to increase quality—clinical teams are expected to do more with less. While many of these groups look to improving clinical resources and tools or optimizing processes, more and more are evaluating the implementation of electronic tools to increase clinical trial efficiency—most notably in the form of electronic trial master file solutions like eTMF Connect.

"CROs play an increasingly critical role in the execution of clinical trials, and have emerged as integral stakeholders in the compilation of Trial Master Files and electronic submissions," said Paul Fenton, President & CEO of Montrium. "We are extremely excited to have been selected as a strategic partner of EastHORN to help them empower their continued growth. Partnering with another forward-thinking CRO such as EastHORN attests to the growing traction our eTMF platform is having in the market."

Upcoming Events

  • 26Jan

    Reducing Complexity in Starting Clinical Trials – More Patients, Faster Startup

  • 27Jan

    Medical Device Clinical Trials in China: Latest Regulatory Developments

  • 11Feb

    Lab X.0: Addressing Quality and Compliance Challenges in Laboratory Operations in the COVID-19 All-Digital Era

  • 23Mar

    Data Integrity for GCP Professionals: Core Requirements, Expectations and Challenges

  • 26Apr

    MAGI's Clinical Research vConference — Spring 2021

Featured Products

  • Regenerative Medicine – Steps to Accelerate Development : PDF

    Regenerative Medicine: Steps to Accelerate Development

  • Clinical Trial Agreements — A Guide to Key Words and Phrases : PDF

    Clinical Trial Agreements: A Guide to Key Words and Phrases

Featured Stories

  • Virtual Doctoer

    Simple Changes Can Make Trials More Patient Friendly

  • Drug approval

    Two-Thirds of Trial Subjects for Drug Approvals Are Outside the U.S.

  • VaccinewithNeedle-360x240.png

    Rules of Vaccine Approval May Be Changing, But Statistical Analysis Tools Remain Constant

  • AskTheExperts-360x240.png

    Ask the Experts: Trial Operations Adjustments in a Remote World

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.

Learn More Here
  • About Us
  • Contact Us
  • Privacy Policy
  • Do Not Sell My Personal Information

Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2021. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing