Emergo can help you implement a vigilance system for adverse event reporting, recalls and post-market monitoring as required by the MFDS.

2 Health professionals or patients report adverse events (AE) after the administration and use of a medicine; the PV team assesses each report and investigates ...

In case you have experienced any adverse event related to the use of Linde Healthcare products and/or services, please fill out the form below with as much ...

Korea Adverse Event Reporting System (KAERS) is an online system designed to facilitate the management of adverse event reports associated with post-marketing ...

We provide end-to-end pharmacovigilance services in South Korea that include adverse drug reaction reporting, signal detection & management, aggregate report ...

The term “Adverse Event, AE” means unintended effects and undesirable signs (e.g. abnormal lab test result), symptoms and diseases that occur during ...

➢ The minimum criteria for an adverse event report to be valid are AE information, drug information, patient and reporter information. ➢ KIDS periodically ...

21 окт. 2024 г. · The Korea Adverse Event Reporting System (KAERS) compiles spontaneously reported adverse event data for medicinal products including herbal ...

21 авг. 2024 г. · South Korea also declared an effective endemic by downgrading the COVID-19 infectious disease crisis alert from “serious” to “alert” on May 11, ...

Reportable Adverse Events. In an occurrence or likelihood of death or a serious side effect, information must be reported to the MFDS by the manufacturer or ...