Post-authorization safety (PAS) studies play a crucial role in ensuring the ongoing safety and effectiveness profile of pharmaceuticals after regulatory approval.The PAS studies monitor products…
In the pharmaceutical industry, we have witnessed a dramatic expansion of the use of real-world data throughout the product’s lifecycle. Currently, real-world evidence (RWE) is…
MedEngine is a digitally-minded, premium partner for the pharmaceutical industry. We act boldly in bridging medical science with business to provide our Nordic and global…