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ACR Monitoring Sub Cadre: CMO Sr. Name of the OfficerDOBEmp. No. Grade/Name of the Institution where working200203 200304 200405 200506 200607 200708 200809 200910 201011 201112 201213GNCT, DelhiNoNoNoNoNoNo1010
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ACR monitoring, also known as adverse event reporting monitoring, is the process of tracking and evaluating adverse events or side effects related to a product or service.
Any company or organization that produces or provides a product or service that may cause adverse events is required to file ACR monitoring reports.
ACR monitoring reports can be filled out electronically through a designated online portal or submitted manually by completing a standardized form.
The purpose of ACR monitoring is to ensure the safety and effectiveness of products and services by monitoring and addressing any adverse events that may occur.
Information that must be reported on ACR monitoring includes details of the adverse event, its severity, any actions taken in response, and follow-up measures.
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