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Medical Device Complaint Handling Systems

Medical Device Complaint Handling Systems - Webinar By GlobalCompliancePanel

Overview: This webinar is intended to demonstrate how to adequately establish and maintain medical device complaint handling systems. All medical device manufacturers are required to comply with the complaint handling requirements. Understanding the relevant and applicable requirement can significantly contribute to achieving compliance and remaining compliant, resulting in saving significant amount of time and efforts in business while ensuring the safety and effectiveness of the medical device products.Why Should You Attend: FDA regulations require all medical device manufacturers to comply with the complaint requirements. This webinar will discuss how to adequately establish and maintain medical device complaint handling systems.Areas Covered in the Session:Overview and review of the applicable statutes and regulationsDefinitionsWhat to do when complaints are received?How to process complaints.What processes need to be in place?When to investigate complaints.When to open a CAPA(s).Contents of records of investigation.Enforcement actions: numerous case studiesLessons learnedWho Will Benefit:CEOsVPsCompliance officersAttorneysComplaint handling personnelClinical affairsRegulatory affairsQuality assuranceR&DCROsConsultantsContractors/subcontractorsPrice: $225.00GlobalCompliancePanelPhone: 800-447-9407Fax: 302-288-6884


6 Mar 2013 @ 10:00 am

6 Mar 2013 @ 11:00 am

Duration: 1 hours

Timezone: GMT -8:00


Online Webinar

Organised by

GlobalCompliancePanel (deactivated)

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