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A licensing seminar for FDA Center for Device Regulation, Radiation Health, and Research stakeholders which aims to provide information on the Rules and Regulations prescribing the requirements and procedures in the application for License to Operate for medical device manufacturers, repackers, traders, distributors, importers, exporters and wholesaler. The topics include the requirements, procedure for Eportal and Eservices Portal Systems covering the initial, renewal and variation applications; as well as the schedule of fees and processing time.

Join our FREE webinar on 03 April 2024 from 8:00 am to 12:00 nn via Cisco Webex
Register through this link:

Maximum of 500 participants
First-come-first served