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. It improves how we run trials. We can use data, AI, and automation to make…
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,…
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…
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 medical device clinical studies. To maximize the benefits, clinical trial sponsors should follow expert-recommended best…
In recent years, technology has been playing a central role in healthcare and clinical research developments. Among these welcomed innovations are electronic Case Report Forms, which are one of the electronic data capture tools that are revolutionizing the way we conduct clinical…
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