Provide guidance and support to internal stakeholders on reporting requirements and processes.
September 26, 2023
Ensure compliance with FDA regulations and guidelines for reporting adverse events related to medical devices.
September 28, 2023
Investigate and gather information on adverse events, including contacting healthcare providers and patients for additional details.
October 05, 2023
Participate in the development and implementation of strategies to improve the reporting and monitoring of adverse events.
October 06, 2023
Communicate with regulatory agencies and respond to inquiries related to adverse event reporting.
October 18, 2023
Stay current on industry developments, regulations, and best practices related to medical device reporting.
October 29, 2023
Document and maintain accurate records of adverse event reports and related communications.
November 05, 2023
Monitor and track trends in adverse event reports to identify potential safety concerns or areas for improvement.
November 18, 2023
Collaborate with cross-functional teams to assess and address potential safety issues with medical devices.
November 24, 2023
Review and analyze adverse event reports related to medical devices to determine if they meet reporting requirements.
November 25, 2023