6-Hour Virtual Seminar on Effective Complaint Handling and Medical Device Reporting

If you are unable to see the message below, [click here to view](. [Logo]( 6-Hour Virtual Seminar [6-Hour Virtual Seminar on Effective Complaint Handling and Medical Device Reporting]( [REGISTER NOW]( Medical Device Reporting (MDR) compliance involve regulatory obligations and proper and timely reporting. Failure to properly report events can cause costly problems for a manufacturer and can be life threating for consumer. Date: Tuesday, February 25, 2020 Time: 08:00 AM PST | 11:00 AM EST Duration: 6 Hours Instructor: Rita Hoffman Overview: Complaint Handling and Medical Device Reporting (MDR) are a part series on Post Market Compliance for medical device manufacturers. The FDA is continuing their efforts to issue numerous FDA Warning Letters and serious enforcement actions, including criminal & civil penalties levied on companies that failed to properly report events and take proper corrective or preventive actions.[Read more..](. Who Will Benefit: - Regulatory Affairs - QA/QC - Project Managers - Regulatory Professional - Risk Managers - Complaint Handling Teams - CAPA Teams About Speaker: Rita Hoffman Owner, Regs & Recall Strategies Rita Hoffman is the Principal Consultant/Owner of Regs & Recall Strategies, LLC, and a consulting firm providing regulatory insight focusing on industry assistance on FDA compliance issues. Ms. Hoffman has been consulting with FDA firms on post marketing issues for the past 6 years. [Read More]( GlobalCompliancePanel 39658 Mission Boulevard, Fremont, CA 94539, USA. Toll Free: +1-800-447-9407 Fax: 302 288 6884 [www.globalcompliancepanel.com]( | [Unsubscribe]( Copyright © 2020 GlobalCompliancePanel. All rights reserved.