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.

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