An adaptive design to optimize clinical investigation
The quality of a clinical trial design is essential to ensure participant safety and obtain robust conclusions […]
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Master protocol: structuring pillar for clinical investigations.
A common architecture for several clinical investigations, the master protocol is beginning to be used in the medical device sector. The
Master protocol: a pillar for structuring clinical investigations. Read more "
How do I find a job after training at ARC?
Clinical research associate (CRA) training is an essential step in entering the clinical research field. It allows you to acquire the technical and regulatory skills necessary to oversee clinical trials. But once you have completed your training, a question often arises: how do you find a job?
After training at ARC, how do you find a job? Read more "
MDR Regulation: everything you need to know to write a compliant PSUR.
The new European regulation on medical devices requires the drafting of a periodic safety update report, or PSUR, a process
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The importance of biostatistics in clinical research
Biostatistics plays a crucial role in human health studies. This mathematical science of data transforms
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Continuing education: a lever for eco-responsibility in healthcare
Adopting eco-responsible behavior requires optimized human resources management and support for employees as they progress in their careers.
Continuing education: a lever for eco-responsibility in healthcare Read more »
Digitization for decarbonization: myth or reality?
In medicine and more broadly in healthcare, the transition to digital processes and systems is often seen as
Digitization to reduce carbon emissions: myth or reality? Read more »