Drug development is becoming more global and the need for standardized safety monitoring practices is undeniable. The increased complexity of…
Passed in 2016, the 21st Century Cures Act (The Cures Act) (1) introduced changes intended to increase medical research funding…
Clinical trials are a process in the healthcare world that has been happening for a long time. They play an…
New and advanced drug research has been carried out more and more in recent years because of the constant advancement…
In the realm of modern healthcare, personalized medicine emerges as a groundbreaking approach, heralding a new era in the way…
An ECRF (electronic case report form) is the digital counterpart of traditional paper-based case report forms used in clinical trials….
The regulations for medical devices are constantly changing because they reflect ongoing innovations and safety standards. These changes have significant…
In the third quarter of 2023, the global digital health funding landscape experienced a significant shift, with a notable drop…
In recent years there have been multiple revisions and new additions to regulations concerning technologies in the healthcare industry. With…
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