PATIENT DATA REPORTING WHITE PAPERS & ARTICLES

PATIENT DATA REPORTING APPLICATIONS & STUDIES

PATIENT DATA REPORTING PRODUCTS & SERVICES

Are you anticipating rapid growth, getting ready for an equity event, or coming off a legacy system? NetSuite ERP’s all-in-one cloud business management solution helps future-proof your organization, eliminate redundancies and data silos, and automate manual processes, so you’re always ready for your next business milestone.

The success of clinical trials depends on patient participation.

But patients and caregivers need reliable support first.

Being part of a trial is often nuanced and time-consuming. Archaic travel, antiquated payment processes and card fees are not only frustrating, but can also chip away at the reimbursement funds participants are owed.

This isn’t what you want for your participants, but you haven’t had a better choice. If we have the technology to make things better, we should. So we are.

Mural Link is the clinical research industry’s first participant management platform, designed to meet the needs of modern-day participants, help them enroll and remain in a trial, and reduce the administrative burden for sites.

Ergomed’s Meticulous Risk-Based Quality Management Approach

As a pioneer in providing comprehensive support for your clinical research, Ergomed champions an innovative Risk-Based Quality Management (RBQM) approach. This forward-thinking strategy ensures the highest patient safety standards, regulatory compliance, and data reliability. Ergomed’s proactive approach to managing clinical trials tackles clinical research complexity head-on.

The most widely trusted solution for clinical trial disclosure management

Managing clinical trial disclosures can be tedious and error-prone, opening the door to noncompliance. TrialScope Disclose provides a better way.

Our centralized platform automates data entry and reporting for Clinicaltrials.gov, CTIS, and more. This reduces manual effort so you can focus on bringing new treatments to patients, not paperwork.

Our model combines the depth and experience level of our people with effective tools and processes already in place that are designed to ensure your critical eTMF documents and content are secure, organized, readily accessible, and always in complete compliance with all relevant regulations.

Our research is powered by MRN owned, regulatory-approved and validated eClinical software systems. Our technology can be used at-site and at-home enabling fully integrated data through any clinical trial.

Discover why more life science teams are using OpenClinica Unite™ to automate source data acquisition from patient medical record systems to clinical trial research databases and case report forms.

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