Leveraging technology to automate the contracting process.

Transforming Clinical Trials and Site Contracting

The success of a clinical study is dependent on a multitude of critical factors, with one of the most significant being the establishment and maintenance of strong relationships with investigator sites.

Understanding the Intricacies of Site Start-up

Initiating a new site involves several stages, each with its unique set of requirements and potential bottlenecks, as depicted in Figure 1. From site selection and contract negotiation to site training and patient recruitment, the process is extensive and can be impacted by any number of delays at each of these stages. Each of these stages requires substantial time and resources, which cumulatively contribute to the lengthy start-up time.

An innovative method for feasibility and site selection

Employs specialized automated technology and advanced analytics to collect essential data for informed decisions on trial strategy, protocol finalization, and optimal site selection. This cloud-based solution accelerates critical timelines and enhances communication and collaboration between sponsors and sites.

Survey Design

Standardize and re-use survey questions and leverage advanced survey review capabilities to improve collaboration.

Site Outreach

Better orchestrate site outreach and increase transparency into survey status for efficient follow-up.

CDA Workflow

Automate workflow with eCDAs, in-tool document CDA negotiation, document exchange and tracking.

Survey response

Streamlined delegate assignment and survey pre-population speeds site response.

Analysis & Selection

The optimization of delegate assignment and survey pre-population enhances site responsiveness.

Dashboard

View actionable insights from dashboard and export real-time reports at site, country or study level for further analysis.

Ease the burden for both sites and sponsors

ECLEVAR Milo ’s cloud-based site contracting solution helps sponsors shorten completion timelines, improve the site and investigator experience and gain more clarity and better oversight.

Digitally transform cumbersome feasibility assessments.
Automate to reduce repetitive, manual data entry.
Overcome the barrier of disparate systems that prevent integration and heighten risk.
Optimize portfolio or study planning, support protocol and study design and select the sites which give your study the best chance of success.
Ensure your study enjoys site satisfaction and on-target enrollment

Over 43 MedTech Companies Trust MILO

Get Started with Milo Today

Transform your site contracting process with Milo’s advanced platform. Contact us today to learn more about how Milo can help you streamline your clinical trials and achieve faster, more efficient results