Device Reporting Web-based Seminars

Regulatory Complaint Handling MDRs Recalls - Webinar GlobalCompliancePanel Overview: Medical device firms need to be aware of the benefits of compliance as well as the dangers of inadequate complaint handling. This Webinar will explain the regulatory process and in understandable terms. Tuesday, July 3, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Update on Unique Device Identifier for Device Manufacturers - Webinar By GlobalCompliancePanel Overview: Recent reports identified several potential benefits to widespread use of UDI, such as reducing medical errors, facilitating recalls, improving medical device reporting, and identifying incompatibility with devices or potential allergic reactions. Tuesday, May 22, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Medical Device Reporting Regulations and Violations - Webinar By GlobalCompliancePanel ...Device Reporting regulations and common violations leading to Warning Letter filings by FDA. As part of the review, actual Warning Letter and FDA-483 citations of small and large medical device manufacturers will be explored for Medical Device Reporting issues. There is a great deal of concern at FDA over the quality of the information being reported and the timeliness. Some at FDA are  more...