Adverse Event Reporting News

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With FDA poised to introduce a new “safety reporting rule” for drugs and biologics and with ever increasing emphasis on minimizing medication errors, FDA inspectors are focusing more on complaint handling and corrective action. With this in mind, we created a news service devoted EXCLUSIVELY to adverse event reporting regulation.

Adverse Event Reporting News is the first and only publication that covers adverse events, including ADRs, MDRs, vaccines and dietary supplement, and vigilance reporting regulatory news from the European Union. It's your best solution for avoiding problems with FDA and foreign regulatory agencies.

You receive:

* A biweekly publication in PDF format that you can distribute throughout your company or post on your intranet without penalty of copyright violation.
* Discounted access to adverse event reports from FDA through our RECORD-RETRIEVE Service--we file FOIA requests for you!
* Information on which firms--competitors, clients and suppliers--are getting cited in warning letters and 483s for complaint handling and AE reporting failures.
* News from the EU on vigilance.
* Insight on how FDA will regulate safety reporting and MDRs.
* Information on which firms are trying to get copies of the reports you filed with FDA.
* FDA MedWatch and labeling updates.

You can receive an electronic license for Adverse Event Reporting News (24 issues), which can be distributed throughout your company, for $1499---If you don’t want an electronic license, simply order at the individual copy rate of $865.00.

Order a full license today and get a FREE copy of "The Guide to Vigilance and Adverse Event Reporting." Get all current FDA and EU guidance and regulations governing pharmacovigilance and medical device reporting -- all in one handy guide. Regular price is $487, but is yours FREE with your order today!

Click here to order online or call 703.779.8777.

For any questions or concerns please call 703.779.8777 or email service@fdainfo.com.