The introduction of the European legal framework for medical devices through the Medical Device Regulation (MDR) and the In-vitro Diagnostic Medical Devices Regulation (IVDR) has increased the requirements
Pharmacovigilance/vigilance (PV) plays a central role in the pharmaceutical industry. It refers to the monitoring of medicines and medical devices after their approval,
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Everyday PV life with evalii® at Cross4Channel Welcome to our look behind the scenes at evalii®! Interview about monitoring pharmacovigilance (PV) at Cross4Channel GmbH
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Pharmacovigilance, i.e. monitoring the safety of medicines and recording side effects, is a major challenge in today's digital world.
The safety and effectiveness of medical devices are of crucial importance for modern healthcare worldwide. In addition to post-market surveillance, vigilance plays a central role.
Digital transformation has reached the pharmaceutical industry and is revolutionising the way drug safety is monitored. In particular, the use of artificial intelligence (AI)
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