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Live Webinar on FDA Adverse Event Reporting for Drugs and Medical Devices

This web seminar presents an overview of FDA

This web seminar presents an overview of FDA’s Adverse Event Reporting Systems for Drugs and Medical Devices. Adverse Event Reporting for Investigational Drugs/Medical Devices and post-approval Adverse Event reporting will be covered. Attendees will receive information about FDA Adverse Event regulations and how to interpret and comply with the various regulations.This is a must attend webinar for those personnel that require an understanding of the regulations governing  FDA’s Adverse Event Reporting for Drugs and Medical Devices.Areas Covered in the Session :FDA Adverse Event Reporting SystemsInvestigational Adverse Event ReportingMarketed Product Adverse Event ReportingAdverse Reporting DefinitionsSafety Reports and Unexpected Adverse Device EffectsWho Will Benefit:Regulatory Affairs PersonnelQuality PersonnelClinical PersonnelResearch PersonnelLaboratory PersonnelManufacturing PersonnelLegal PersonnelAuditorsClinical Research AssociatesPersonnel who require a general understanding of the FDA’s  Drug and Medical Device Adverse Event Reporting requirements.Price Tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, CanadaCustomer Support : #416-915-4458


27 Aug 2014 @ 01:00 pm

27 Aug 2014 @ 03:00 pm

Duration: 2 hours

Timezone: GMT -8:00


Online Webinar



Organised by

Compliance Trainings (deactivated)

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