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Webinar On Complaint Handling & Medical Device Reporting (MDR)

This presentation is intended to help global medical device firms and stakeholders adequately implement US FDA-compliant medical device complaint handling and medical device reporting (MDR) systems.

On Going Christmas Offers: Offer valid till 1 st January 20151. Register an attendee for Single Live:Get 10% of on every RegistrationFirst 10 attendees will receive recording Access to the webinar for No Additional CostFor Coupon Code call customer support:  416-915-44582. Register your Group for Corporate Live:Get 15% of on every RegistrationEvery group registrant will receive Recording Access to the webinar for No Additional CostFor Coupon Code call customer support: 416-915-44583. Unlimited viewing for 4 days4. The discounted amount will appear after entering the Coupon Code in the Secure Check Out PageDescription:This presentation is intended to help global medical device firms and stakeholders adequately implement US FDA-compliant medical device complaint handling and medical device reporting (MDR) systems.  Even if it is believed that the similar or relevant procedures have been implemented in your firms, it is time to ensure all aspects of the requirements are under check to be adequate and compliant. To achieve compliance and to remain compliant with the FDA-compliant complaint handling and medical device reporting, it is imperative that the firms accurately understand, interpret, and implement the requirements for handling all complaints (electronic, written, or ORAL) and medical device reporting to be better sustainable as evident from a recent case. Areas Covered in the Session :Applicable Laws and RegulationsDefinitionsRequirements for Complaint HandlingRequirements for Medical Device ReportingApplicable Processes and ProceduresKey Elements in the Procedures: Complaint Handling and MDRWhat to Do When a Complaint Is ReceivedWhat/How/When to Investigate a ComplaintComplaints Investigation and DocumentationMedical Device ReportingHow to Determine Reportable EventsWho Will Benefit:Complaint ManagersRegulatory AffairsQualityClinical AffairsR&D engineers and scientists, managers, directors, VPsCompliance and Legal AffairsCROAuditors and ConsultantsSenior ManagementAnyone Interested in Medical Device Complaint Handling SystemsFor more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada  Customer Support : #416-915-4458   

When

16 Jan 2015 @ 01:00 pm

16 Jan 2015 @ 02:00 pm

Duration: 1 hours

Timezone: GMT -5:00


Where

Online Webinar


Organised by

Compliance Trainings (deactivated)

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