|Quantity Discounts||1 - 9999|
|1 - 9999|
|1 - 9999|
With increased staffing, the agency has doubled the number of establishment inspection reports reviewed, from 215 in 2006 to 416 in 2011.
As heightened inspections — and warnings — become the “new normal,” it’s vital to know what’s triggering citations and what to do if you’re hit with a Form 483.
In fact, the more you know about how to handle 483s, the more power you have to handle things without facing subsequent warning letters, consent decrees … and even recalls.
Now, FDAnews helps you mount a timely, effective response to keep inspection citations from leading to further costly consequences.
Ready-to-use guidance from an expert on
Form 483 and warning letter responses
To provide expert advice on this critical issue, FDAnews has engaged Gordon B. Richman — EduQuest’s Vice President for Strategic Compliance and Consulting and General Counsel — to help attendees learn how to survive in this tough new climate.
In just 90 minutes, he will provide a strategic overview plus industry trends, case studies and ready-to-use advice, including:
A flexible fit for your busy schedule
The Form 483 and Warning Letter Responses webinar is convenient to attend. All that’s required is that you be in front of a screen at the appointed time, whether you’re at the office or telecommuting from your office-in-home.
Of course, Mr. Richman will be on hand to answer all of your questions. Simply submit your questions via email, and you’ll have answers by the time the session ends.
Everyone in your organization — from compliance officers and general counsel to quality assurance and risk management specialists — will benefit from taking part in this event. Best of all, everyone can do so at a cost that won’t break the budget. You pay one single low registration fee per facility, regardless of how many participate. So spread the word.
|Date:||Sept. 26 – Oct. 14, 2011|
|Location:||Your office or conference room (no need to travel!)|
Gather your team for maximum benefit! Your investment is for one dial-in.
Significant tuition discounts are available for three or more sites from
Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally
We accept American Express, Visa and MasterCard. Make checks payable to FDAnews.
Or, register by phone: toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600
Registrations may not be cancelled. Please contact customer service to make any substitutions.
Interested in Becoming a Speaker?
We're always looking for industry leaders eager to share their expertise at an FDAnews audioconference, webinar or physical conference. Our seasoned speaker community includes executives in the pharmaceutical, medical device and clinical trial industries, regulatory affairs, quality control, compliance, healthcare and academia, as well as several former — and current — top FDA officials. Click here to complete our speaker opportunity form and have a representative contact you about future opportunities.
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