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Explore our insights into Phase 4 Trials, where we ensure drug safety and efficacy through vigilant post-marketing studies and real-world evidence.

Clinical Trials

Understanding Our Role in Phase 4 Trials

Overview of Phase 4 Trials Phase 4 Trials play a key role after a new treatment gets regulatory approval. They keep checking the treatment’s performance,

Clinical Trials

Clinical Trial Feability: Ensuring Success & Efficiency

Understanding Clinical Trial Feasibility Clinical trial feasibility means evaluating if a clinical trial can be done successfully. It involves looking into if there are enough

Compliance

Clinical Evaluation Report Insights and Guidelines

Understanding the Clinical Evaluation Report The Clinical Evaluation Report (CER) reviews medical devices for safety and how well they work. It’s key for getting regulatory

Clinical Trials

RWE Clinical Trials: Insights & Outcomes

Introduction to RWE Clinical Trials RWE Clinical Trials are changing healthcare by using many kinds of real-world data. They use information from electronic health records

Unlock effective strategies to streamline Clinical Trial Patient recruitment and enhance enrollment rates for your studies.

Clinical Trials

Effective Strategies for Clinical Trial Patient Recruitment

Engaging and Retaining Participants Keeping participants engaged and retained is key in successful clinical trials. At Milo, we start by making sure the recruitment experience

Clinical Trials

Optimizing Clinical Record Trial Site Selection Success

The Importance of Effective Clinical Trial Site Selection Choosing clinical trial sites is crucial. It affects everything from costs to how well we can recruit

Elevate your clinical trials with professional medical writing services, ensuring accuracy and regulatory compliance.

Digital Health

Expert Medical Writing for Clinical Trials

Medical writing for clinical trials is all about creating important documents. These documents are key for a trial’s success. You need to pay a lot

Optimizing Site Selection for Clinical Trials

Choosing the right sites is key to clinical trial success. By looking at past problems and using data, finding sites gets easier. It helps speed

Unlock optimal outcomes with our expertise in Site Identification clinical trial strategies, ensuring success in your research endeavors.

Digital Health

Site Identification Clinical Trial Experts

Finding expert sites for clinical trials is key to success. Using IQVIA’s Connected Intelligence, specialists can find the best recruiters. This helps bring more people

Explore the role of a clinical research coordinator and unlock career opportunities in guiding pivotal healthcare studies.

Digital Health

Clinical Research Coordinator: Your Study Guide

A Clinical Research Coordinator (CRC) plays a key role in clinical trials. They work closely with the Principal Investigator (PI). Their job is to make

Uncover the edge in clinical research with our digital CRO clinical trial solutions, enhancing efficiency and patient engagement.

eCRF

Optimizing Digital CRO Clinical Trial Success

The FDA approval process is very tough. Only about 7.9% of new medicines get approved. Using digital CRO clinical trials can help us do better.

Compliance

Understanding eTMF Systems for Clinical Trials

eTMF systems are critical for managing clinical trial stages. They make sure that documents are handled securely and in compliance with the law. These systems

Explore how we enhance patient engagement and satisfaction through our commitment to patient centicity in clinical trials. Join the evolution with us.

Digital Health

Patient Centricity in Clinical Trials: Our Approach

Our method highlights the importance of patient needs in clinical trials. In the healthcare world today, putting patients first is crucial. Technologies like telehealth and

Explore the critical role of doctor signatures in healthcare and learn about their legal requirements, authentication, and implications for patient care.

DCT

Understanding Doctor Signatures: A Guide

Doctor signatures are key in the healthcare world. They mark approval and authority from medical professionals. Physician signatures confirm services, review records, and are needed

Join us at Alcoa Clinical Research for cutting-edge medical studies and help shape the future of healthcare. Contribute to scientific breakthroughs.

Clinical Trials

Alcoa Clinical Research: Advancing Medical Science

Alcoa Clinical Research leads in cutting-edge medical science. We run detailed clinical trials and studies at our top-notch research facility. By focusing on new drug

Explore how Hybrid Clinical Trials are reshaping medical research, offering a blend of traditional & modern methods for enhanced outcomes.

DCT

Hybrid Clinical Trials: Revolutionizing Research

We’re thrilled about the huge impact hybrid clinical trials can make. These trials, also called virtual or decentralized trials, are changing how we do clinical

Clinical Trials

Optimizing Your Partnership with CROs and Outsourcing

With the advancement of technology and regulatory obligations in medicine, research institutions are facing obstacles to maintain their R&D efforts for new therapeutics. As a

Studies have indicated that CROS and BiCROS hearing aids offer noteworthy advantages to individuals suffering from auditory impairment, such as better listening capabilities amidst noisy settings and an effortless user experience.

Digital Health

Exploring the Use of CROS and BiCROS Hearing Aids in Clinical Research

Many individuals worldwide experience hearing loss as a widespread condition. The World Health Organization (WHO) has projected that by 2050, one out of every four

The process of clinical research is intricate and crucial, involving multiple parties to ensure the prompt delivery of optimal investigational treatments to patients.

Clinical Trials

CRO vs. Sponsor, An Overview about Differences

The process of clinical research is intricate and crucial, involving multiple parties to ensure the prompt delivery of optimal investigational treatments to patients. Following disruptions

Heart diseases affect a significant part of the population, causing 1 in 5 deaths in the USA, as estimated by the Centers for Disease Control and Prevention (CDC).

Clinical Trials

The Development of New Drugs for Cardiovascular Disease

Heart diseases affect a significant part of the population, causing 1 in 5 deaths in the USA, as estimated by the Centers for Disease Control

Duchenne muscular dystrophy (DMD) is a rare genetic disorder that disproportionately affects males, with an incidence of 1 in 3600 male infants.

DCT

Key Strategies for Successful Development of Duchenne Muscular Dystrophy Clinical Trials

Duchenne muscular dystrophy (DMD) is a rare genetic disorder that disproportionately affects males, with an incidence of 1 in 3600 male infants. The disorder is

A query is a communication tool used in the clinical trial process to clarify or resolve any discrepancies or inconsistencies found in the data.

EDC

Understanding Query Management

A query is a communication tool used in the clinical trial process to clarify or resolve any discrepancies or inconsistencies found in the data. Finally,

Source Data Verification (SDV) is a method that clinical research organizations (CROs) can use to ensure the data they’re gathering is accurate.

Clinical Trials

Clinical Trial Basics: Source Data Verification (SDV)

Source Data Verification (SDV) is a method that clinical research organizations (CROs) can use to ensure the data they’re gathering is accurate. It involves comparing

The total number of DCTs has increased more than fivefold worldwide, from 250 trials in 2012 to 1,291 in 2021.

Clinical Trials

Understand the prominence of CNS being the most researched therapeutic area of DCT trials

The evolvement of digital technologies in the past years has been transformative in the field of clinical trials in therapeutic areas, being CNS (Central Nervous

Discover leading support with our preclinical contract research organization, your partner in advancing drug development efficiently.

DCT

Premier Preclinical Contract Research Organization

Our Premier Preclinical Contract Research Organization is at the forefront of revolutionary drug development. We use the advanced MILO digital platform to meet diverse preclinical

Streamline your studies effortlessly with our powerful clinical trial database software, enhancing efficiency and data accuracy.

Clinical Trials

Optimize Research with Clinical Trial Database Software

MILO is a top digital platform that specializes in decentralized clinical trials. It provides an all-inclusive clinical trial database software. This software aims to improve

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

DCT

Optimizing eSource Clinical Trials 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

Explore our EDC database solutions tailored for seamless clinical trial data management to enhance accuracy and efficiency.

Digital Health

EDC Database Solutions for Efficient Data Management

At MILO, we are experts in advanced EDC database solutions. These are designed to make managing clinical trial data simpler. Our platform has everything needed

Monitoring

Optimizing Remote Monitoring Clinical Trials Safety

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

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

Compliance

IWRS Randomisation: Streamline Clinical Trials

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

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

DCT

Optimizing eTMF Documentation for Clinical Trials

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,

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.

eConsent

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

Clinical Trials

An overview of Decentralized Clinical Trials

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

Clinical Trials

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. COA is an electronic

Case Report Form (CRF) is an electronic or paper document that is used in a clinical trial to record the protocol and required information about each participant.

eCRF

Expert Insights on CRF Clinical Research Practices

Comprehending the best practices in clinical research is the best way to evolve and be updated to participate in the ever-transforming realm we are part

Delve into the vital significance and comprehensive services offered by Electronic Data Capture (EDC) systems in revolutionizing clinical trials.

DCT

Significance & Services of EDC Systems in Clinical Trials

EDC (Electronic Data Capture) system is transforming the field of Medtech and clinical trials in an unparalleled way. This software solution allows medical device companies

Unlock the potential of EDC signification (electronic data capture) for efficient clinical data management and streamlined research processes.

DCT

Unlock Insights with MILO EDC Data Solutions

The realm of clinical research has been deeply changed, mainly the way we collect and manage data, with the surge of Electronic Data Capture (EDC).

PMCF

Tips for PMCF Planning

It’s paramount to keep the pace of preparation activities in Post-Market Clinical Follow-Up (PMCF) planning, since the MDR has drastically enhanced the bar for supporting

A PMCF Plan is a paramount technical document that highlights a method for conducting Post Marketing Clinical Follow Up on a medical device

Clinical Trials

How to write a comprehensive PMCF Plan for medical devices under the Medical Device Regulation (MDR)

The medical device field is always evolving and post-market clinical follow-up (PMCF) has become a critical area of focus for manufacturers. A PMCF Plan is

Electronic consent (e-consent) is another method of obtaining informed consent through the use of an electronic system instead of a paper consent form, e.g. in REDCap or DocuSign

Clinical Trials

Understanding Remote and Electronic Consent (e-Consent)

When the study team and participant are not in the same physical location during the consent process, the use of Remote Consent became pivotal. Remote

Clinical Trials

Participate in At Home Clinical Trials Safely

Remote clinical studies, also called virtual research trials, enable people to easily and safely take part in medical research from the comfort of their own

Hybrid Clinical trial

Navigating Hybrid Clinical Trials: A New Era

The age of hybrid clinical trials has come up, integrating traditional procedures with digital advancements to transform medical research. These contemporary style trials mix the

Explore the latest in clinical trial technology to streamline your research and enhance patient outcomes. Discover next-gen solutions with us.

Clinical Trials

Navigating Remote Clinical Trials: Our Expertise

The currency of remote clinical trials rise significantly after the COVID-19 pandemic. The method provides a practical solution for overcoming challenges proposed by traditional systems,

PMCF

Importance of Post-Market Clinical Follow-up in Medical Regulation

Post-market Clinical Follow-up involves collecting clinical data on medical device conducting and safety post-market. It establishes continual observance, identifying any accidental complications or risks. PMCF

ePRO

ePRO vs eCOA: Key Differences Explained

Distinction between ePRO vs eCOA Electronic Clinical Outcome Assessments (eCOA) and Electronic Patient Reported Outcomes (ePRO) are two types of methods of data gathering in

Discover how clinical trials apps are revolutionizing patient engagement and research efficiency in the digital age of health innovation.

DCT

Exploring Clinical Trials Apps for Health Innovations

Digital health technologies (DHTs) have emerged as a transformative innovation for the field of clinical trials showing new and amazing possibilities. Including mobile apps and

Unlock the pivotal role of EDC in Clinical Data Management: streamlining data collection, ensuring quality, and expediting clinical trials

EDC

The Importance of EDC in Clinical Data Management

In the ever-evolving landscape of medical technologies, the rise of EDC (Electronic Data Capture) enhanced the conducting of advanced clinical studies. These systems have revolutionized

Streamline your clinical trials with our advanced electronic data capture systems for enhanced accuracy and efficiency in data management.

EDC

Optimizing Trials with Electronic Data Capture Systems

In today’s digital age, electronic data capture (EDC) systems have emerged as game-changers in the world of clinical trials. By leveraging advanced technology and data

eCRF

eCRF Creation Clinical Study: Optimize Trials

Transitioning from paper-based data capture to electronic case report forms (eCRF) improves the quality of data collection, lowers costs, and improves the overall efficiency of

DCT

Benefits of Decentralized Clinical Trials

Clinical trials are the backbone of medical research, open the way for groundbreaking discoveries and innovative treatments. However, traditional clinical trial methodologies often come with

DCT

Advancing Urology with Decentralized Clinical Trials

The introduction of decentralized clinical trials (DCTs) in the field of urology created a transformative environment and triggered a crucial shift. Distancing from conventional research

Compliance

Understanding the Landscape of Urology Regulatory Compliance

The first step and challenge that players inside the urology field envisage is the endeavor to attain regulatory submission approval within the field of urology,

Televisit

Telemedicine for Urology: Expert Care Online

The innovation of telemedicine for urology healthcare is revolutionizing the relationship between patients and doctors. By embracing the technological advancements of telemedicine, individuals in need

Patient Survey FDA Insights & Healthcare Trends

The Healthcare landscape has been facing unprecedented evolution, and monitoring and evaluating the safety and effectiveness of medical products is pivotal. The FDA has long

Mobile E-Diary: Revolutionizing Dermatology Clinical Trials Through Innovative Data Collection

Regarding the constantly developing landscape, especially within dermatology, the accurate monitoring of patient-reported outcomes and treatment adherence is paramount. Thus, traditional methodologies, such as paper-based

In-response-to-the-rising-interest-especially-within-digital-health-and-software-as-a-medical-device-sectors-integrating-continuous-device-data-with-Electronic-Data-Capture-EDC-system

EDC

Exploring the Emergence of EDC Medtech in Healthcare

With the medical technology landscape development, the rise of EDC Medtech leveraged the conducting of advanced clinical studies. EDC (Electronic Data Capture) Medtech has emerged

ePRO

ePro: Direct Data Capture Modules For Medical Devices Clinical Trials

For many types of medical devices – particularly those at the lower end of the risk scale, Direct Data Capture from subjects in their home

DCT

Embracing the Future: Meeting Doctors and Patients Where They Are Now

The world has been passing through significant changes and evolution since its beginning. In the past years, especially during and after the pandemic, we have

The Impact of COVID-19 on Urology and the Rise of Telemedicine

With the occurence of the COVID-19 pandemic, the whole world has passed to an unprecedented transformation, in the landscape of urological healthcare wasn’t different and

In the domain of medical research, clinical trials audit stand as the base for advancing healthcare breakthroughs. These trials not only validate the efficacy and safety of potential treatments but also open the way for innovative therapies to reach the patients who need them most. However, ensuring the integrity and reliability of clinical trial data is fundamental, underscoring the crucial role of audit procedures in the optimization of these trials.

DCT

Optimizing Clinical Trials Audit: Practices for Better Procedures

In the domain of medical research, clinical trials audit stand as the base for advancing healthcare breakthroughs. These trials not only validate the efficacy and