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 caused by COVID-19 in 2020, there has been a steady rise in industry-sponsored trials since…
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). However, cardiovascular conditions are not modern medical concerns. Even Egyptians from 3,500…
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 a study’s source data against its final report, enabling for the identification of any errors…
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 System) in highlight. The introduction of digital endpoints has transformed how, for example, neurodegenerative symptoms…
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 the research process. Our wide array of services includes ePRO, eConsent, EDC, eCRF, eCOA, and…
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…
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…
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…
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