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POST ID: 5621

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

Region: Canada
Location: Mississauga, ON


This is a must attend webinar for those personnel that require an understanding of the regulations governing FDAs Adverse Event Reporting for Drugs and Medical Devices.
Areas Covered in the Session :
FDA Adverse Event Reporting Systems
Investigational Adverse Event Reporting
Marketed Product Adverse Event Reporting
Adverse Reporting Definitions
Safety Reports and Unexpected Adverse Device Effects
Who Will Benefit:
Regulatory Affairs Personnel
Quality Personnel
Clinical Personnel
Research Personnel
Laboratory Personnel
Manufacturing Personnel
Legal Personnel
Clinical Research Associates
Personnel who require a general understanding of the FDAs Drug and Medical Device Adverse Event Reporting requirements.
Price Tags:
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email :

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