Date :
Place : United States, Philadelphia
Contact Person:Event Manager
Description:
Customer satisfaction plays a significant role in measuring a product's postmarket performance. It is an indicator of how effective the product performance is managed. Both the quality system regulation (QSR) and the International Organization for Standardization (ISO) require procedures and processes to monitor and control your post market problems. The complaint-handling mechanism not only collects feedback from unsatisfied customers, but also provides means for failure investigations and subsequent corrective and preventive actions (CAPA).Deadline for abstracts/proposals : 25th October 2018
Organized By :NetZealous LLC - DBA GlobalCompliancePanel
Keynote Speakers : Rita Hoffman Owner, Regs & Recall Strategies Ms. 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. She enjoys teaching firms on how to think like and FDA Officer and shares her skills on her past experiences both in and out of FDA. Prior to working as a co
Conference Highlights :Day 1 Schedule Lecture 1 (90 Mins): Complaint Handling and FDA Expectations Lecture 2 (90 Mins): Medical Device Reporting Procedures (MDR) Procedures and Regulations MDR reporting by firm, agents and exemptions Lecture 3 (90 Mins): Standard Operating Procedures, Guidance Documents Update and eMDR Discussion Ways FDA works with Counterparts What to expect from the Inspector Lecture 4 (90 Mins): Recalls, Definition and Legal Authority Overview Being Recall Ready Day 2 Sched
Venue :DoubleTree by Hilton Hotel Philadelphia Airport, Island Avenue, Philadelphia, PA, USA
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