The Medical Device Coordination Group (MDCG) wants to harmonize adverse events reporting for surgical mesh implants across EU member states. Over the past decade, there have been reports of adverse ...
Per federal regulations, University and affiliate researchers must notify the IRB of unanticipated problems that involve risks to participants or others (henceforth referenced as Unanticipated ...
The US Food and Drug Administration (FDA) has announced that starting on 1 October 2026, manufacturers must submit adverse ...
The rationale for the new obligations is to encourage information sharing between healthcare facilities and the TGA, to ...
The Journal of Clinical Oncology podcast, hosted by Dr. Davide Soldato, presents analyses and discussions centered on the latest findings published in ASCO’s esteemed Journal of Clinical Oncology.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results