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Differing device regulation between regions causes trial challenges
Medical Devices includes a session from a regulatory expert on how companies can align their research between regions.
Understand which barriers to cancer trial participation remain most difficult to overcome, including geography and trial ...
The FDA’s new draft guidance on Bayesian methodology signals a shift toward more flexible, data-driven clinical trial designs, enabling sponsors to use prior data and adaptive approaches to improve ...
KING OF PRUSSIA, Pa.--(BUSINESS WIRE)--Leading clinical trial software solutions innovator Greenphire has just released its annual Market Trends survey sharing invaluable insights from nearly 400 ...
This public workshop provided a venue for stakeholders to consider opportunities for a modern, patient-centric clinical trials enterprise in light of digital health tools that could allow ...
With populations aging, chronic diseases becoming more prevalent, and global health experts warning of potential pandemics, the need for rapid therapeutic development has reached unprecedented levels.
Clinical trial research, like medicine more generally in the European Union (EU), is regulated by a network of national competent authorities from each of the Member States of the European Economic ...
Expertise from Forbes Councils members, operated under license. Opinions expressed are those of the author. In the last decade, the volume of clinical trial data has surged, presenting unprecedented ...
Drugs are man-made miracles. They enhance our health, cure diseases, and extend our lives. However, drug development is not easy. It is a remarkably long, expensive, and complex process. On average, ...
Clinical trials continue to be a driving force in ophthalmology, propelling the development of innovative treatments and ...
Explore key identity management challenges in pharma and biotech SaaS platforms and learn practical solutions for security, ...
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