It is important to understand adverse event reporting. This term is associated with AR-related drug products. Each medical device varies greatly from the pharmaceutical product to the product, as well as product problems, complaints, their occurrence, identification of these cases, reporting regulatory activities, and the requirements of the research after approval.
Other sources get more information on device-specific AE definitions and reporting, product-related issues, and post-marketing research (including logging). This group is associated with AR-related drug products.
A medical device varies greatly depending on the type of pharmaceutical, as well as product problems, complaints, their occurrence, identification of these cases, reporting regulatory activities, and the requirements of the research after approval. Other sources get more information on device-specific AE definitions and reporting, product-related issues, and post-marketing research (including logging). [Continue reading]
