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 of. This field evaluates how effective therapeutic treatments and medical advances are. In this article,…
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 to gather, store, and manage patient data digitally during clinical trials. It optimizes the data…
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). This system plays a pivotal role in unlocking real-world evidence (RWE) by making data collection…
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 data quantity and quality. MILO team has identified frequent problems, each of which, if not…
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 a paramount technical document that highlights a method for conducting Post Marketing Clinical Follow Up…
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 consent using a paper consent form (or remote paper consent) is a specific type of…
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 homes. Such trials rely on digital technology and telemedicine for monitoring participants remotely while gathering…
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 familiar framework of randomized controlled trials (RCTs) with modern trial designs for optimal results. With…
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, like slow recruitment rates and extended data management processes. Milo Healthcare is specialized in handling…
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 helps maintain an acceptable benefit-risk correlation and verifies the intended use of the device. It’s…
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