Live Webinar on FDA Adverse Event Reporting for Drugs and Medical Devices
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.
- (1888PressRelease) July 26, 2014 - 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 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
- Auditors
- Clinical Research Associates
- Personnel who require a general understanding of the FDA's Drug and Medical Device Adverse Event Reporting requirements.
Price Tags:
Live
Single Live : For One Participant = $ 249
Corporate Live : For Max. 10 Participants = $ 899
Recording
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 : support ( @ ) compliancetrainings dot com
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