Adaptive designs allow a clinical trial to be modified based on interim results, while ensuring scientific validity and patient safety.
An adaptive design to optimize clinical investigation Read more »
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 "
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 "
The new European regulation on medical devices requires the drafting of a periodic safety update report, or PSUR, a process
MDR Regulation: everything you need to know to write a compliant PSUR. Read more »
Biostatistics plays a crucial role in human health studies. This mathematical science of data transforms
The importance of biostatistics in clinical research Read more »
The design of a clinical study corresponds to the methodology chosen to conduct a clinical study with a view to answering the following questions
Clinical trial design: innovating to optimize Read more "
If you're a CRA and you don't have enough time to carry out your control visits, you're a
Clinical research: remote monitoring is a reality Read more "
Good clinical practice is evolving to meet today's challenges. ICH E6 R3 introduces key innovations designed to improve
ICH E6 R3: a major turning point in clinical research Read more »
In a context where the health of individuals is closely linked to that of the planet, eco-responsibility is more than just a
Becoming an eco-responsible player in clinical research: initiatives and levers. Read more »
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