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Optimizing eSource Clinical Trials for Efficiency

Unlock the potential of eSource clinical trials with our innovative approaches that streamline data collection and trial management for efficiency.

Moving to fully electronic eSource clinical trials is a big step in modernizing. This change is part of MILO’s vision. They want to make trial processes easier with a digital platform. This platform offers tools like ePRO, eConsent, and more.…

Optimizing Remote Monitoring Clinical Trials Safety

Discover how remote monitoring clinical trials enhance safety and efficiency in our comprehensive guide to virtual trial oversight solutions.

Remote monitoring in clinical trials introduces new protocol designs and better ways of collecting data. The use of decentralized models is growing fast. Because of this, there’s a big need for electronic solutions to support this change. Strong remote monitoring…

Maximize Rewards with Our Copilot Referral Program

Join our Copilot Referral Program and unlock exclusive bonuses! Share your unique link and earn rewards for every successful referral.

MILO introduces a cool referral program. It’s inspired by the famous Copilot money tracker. Our program is a part of our innovative platform for decentralized clinical trials. It fits right in with services like ePRO, eConsent, and more. Our goal?…

IWRS Randomisation: Streamline Clinical Trials

Explore how IWRS Randomisation optimizes clinical trial efficacy, ensuring precise patient allocation and enhanced study integrity.

IWRS Randomisation is changing clinical trials for the better. It makes patient allocation and study management highly organized and efficient. As an Interactive Web Response System, it takes care of many key tasks automatically. These tasks include enrolling patients, keeping…

Optimizing eTMF Documentation for Clinical Trials

Unlock the full potential of your clinical trials with our expert insights into eTMF Documentation strategies for seamless regulatory compliance.

At MILO, we’re changing decentralized clinical trials with our high-tech platform. Our tools help improve clinical research in many ways. These include ePRO, eConsent, EDC, eCRF, eCOA, and RWE. A key part of our work is making Electronic Trial Master…

The Effect of Integrating EMRs into EDC

With the advancements in technologies, the pharmaceutical landscape has been deeply transformed and antiquated methods such as paper-based record have been replaced by electronic record methods.

With the advancements in technologies, the pharmaceutical landscape has been deeply transformed and antiquated methods such as paper-based record have been replaced by electronic record methods. The healthcare industry has also experienced an important shift towards digitalization in the past…

An overview of Decentralized Clinical Trials

Decentralized Clinical Trials (DCTs) indicate a shift towards greater decentralization in clinical research.

Decentralized Clinical Trials (DCTs) indicate a shift towards greater decentralization in clinical research. Consequently, studies are now being conducted across several locations instead of a single centralized site – with an increasing trend in this practice observed. DCTs are applicable…

Significance of eCOA in Clinical Trials

As clinical trials have become increasingly intricate and data-driven, the need for more efficient and accurate data collection has become pivotal.

As clinical trials have become increasingly intricate and data-driven, the need for more efficient and accurate data collection has become pivotal. COA is an electronic data capture process that involves the use of cloud-based systems to collect patient-reported outcomes. eCOA…