新疆乌苏市市场监管局开展“两品一械”不良反应监测培训

Core Viewpoint - The training organized by the Urumqi Market Supervision Administration aims to enhance the monitoring of adverse reactions related to drugs, cosmetics, and medical devices, ensuring early detection and reporting of safety hazards [1][2] Group 1: Training Overview - The training session was attended by 95 participants, including heads and quality personnel from cosmetic and medical device businesses, as well as new market supervision staff [1] - The training was conducted by the director of the Tacheng Region's Adverse Reaction Monitoring Center, focusing on the importance of monitoring adverse reactions [2] Group 2: Regulatory Framework and Responsibilities - The training included a detailed explanation of the "Key Points for Monitoring Adverse Drug Reactions (Medical Device Adverse Events)," emphasizing the necessity of understanding legal regulations [2] - The session aimed to reinforce the reporting responsibilities of monitoring units, ensuring timely identification and reporting of safety issues [2] Group 3: Improvement Measures - The Urumqi Market Supervision Administration plans to enhance supervision of drug, cosmetic, and medical device businesses, conducting regular inspections to create a safe environment [1] - The administration will provide targeted training to improve the quality of adverse reaction reporting and address issues such as inaccurate identification and untimely reporting [2]