We use cookies to provide you with a better experience. By clicking the Accept button, you are agreeing to our use of cookies in accordance with our Privacy Policy.
  • Patient Resources
    • 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
    • Glossary
  • Professional Resources
    • Research Center Profiles
    • Industry Provider Profiles
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • Events
    • Newsletters
    • JobWatch
    • White Papers
    • Patient Education
    • SOPs
  • About Us
  • Contact Us
  • Advertise
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » AG Mednet, Cardialysis partner for efficient cardiovascular clinical trials

AG Mednet, Cardialysis partner for efficient cardiovascular clinical trials

February 28, 2014
CenterWatch Staff

Cardialysis, an independent CRO, has selected AG Mednet, a quality compliance company, as preferred provider for image data submission and collection.

With large amounts of data collected and significant room for data submission errors, there is even greater potential to disqualify participating patients or expose subjects to unnecessary risky procedures due to data errors. With more than 30 years of experience as a full-service CRO and core laboratory specializing in cardiology, Cardialysis has an established network of more than 1,200 sites worldwide and works with pharmaceutical, medical device and biotechnology organizations globally.

“We’re responsible for designing, managing, monitoring and reporting on all aspects of clinical-research trials,” said Teun Smits, manager business development at Cardialysis. “As a CRO with core laboratory services working with AG Mednet, we’re experiencing significant efficiencies and convenience for participating clinical sites, and as such we expect even further improvement in the quality of the data collected and transferred compared to past trials. Electronic data submission and collection contributes to our goal of becoming a fully operated eCRO. ”

AG Mednet provides functionality and support to collect clinical trial image data globally, properly de-identify it to ensure regulatory compliance, apply advanced, automated quality-assurance processes to ensure the data is protocol-compliant and readily usable and deliver it reliably and securely to one or more trial repositories.

“With Cardialysis, we’re working on cardiology-related studies with two major medical device companies and more than 1,000 participating patients,” said Abraham Gutman, president and CEO of AG Mednet.

Global News Technology Solutions CROs/Service Providers
  • Related Directories

    Complion

    IRBNet

    CROMSOURCE

Upcoming Events

  • 16Dec

    Master the Regulatory Pathway for Cell & Gene Therapy Submissions: Strategies for Successful BLAs

Featured Products

  • Regenerative-medicine-steps-to-accelerate-development-pdf

    Regenerative Medicine: Steps to Accelerate Development — PDF

  • Clinical-trial-agreements-a-guide-to-key-words-and-phrases-pdf

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

Featured Stories

  • Ich_logo

    ICH Overhauls 22-Year-Old Clinical Studies Guideline

  • Survey_chart2019

    Sponsors, CROs Doing Better, Sites Say, But More Work Is Needed

  • China-360x240

    U.S. Tops List of Trial Startups With China Making Progress in Phase 1

  • Phoneapp-360x240

    Device Apps Present Unique Risks in Trials

New!

2019 Site Survey Reports

Learn More Here
  • About Us
  • Contact Us
  • Privacy Policy

Footer Logo

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

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2019. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing