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