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

Event Details

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

Time: September 25, 2014 from 1pm to 3pm
Location: Online
Street: 5939 Candlebrook Ct
City/Town: Mississauga, ON
Website or Map: https://compliancetrainings.c…
Phone: 4169154458
Event Type: webinar
Organized By: compliancetrainings
Latest Activity: Aug 27, 2014

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Event Description

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

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