|Quantity Discounts||1 - 9999|
|1 - 9999|
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Who works in the office? What are the staff’s responsibilities? How are they organized? Are they finding and correcting violations? Is it now more expensive to contract with Chinese companies? Is the FDA slowing down imports?
Get the answers to these and many more questions …
In this 90-minute Encore presentation, Raymond Bonner of Sidley Austion, will give you the benefit of his interactions with the FDA staff in Beijing as he explains what they do, what they inspect and what they are finding. In addition, he’ll explain what it means now to outsource to, or import from, China. Sidley Austin is the first international law firm to establish a stand-alone, comprehensive food and drug regulatory practice in China.
If you ever wanted a first-hand account of what’s happening in China, you must register now for this exciting webinar. Sign up your entire team to listen in and discover:
Stop wondering what the FDA’s China office is doing and find out from an expert who knows. Register now and you'll get an opportunity to ask your toughest questions during the Q&A session.
Raymond Bonner is a partner in the Sidley Austin Washington, D.C. office and is chair of the firm's FDA Regulatory and Enforcement practice. He previously served as a federal prosecutor in the District of Maryland for six years, where he prosecuted major pharmaceutical fraud and GMP cases, and litigated other FDA-related cases. He concentrates his practice on FDA -related cases. He has substantial litigation, enforcement, internal investigation, and compliance experience throughout the life sciences industry, particularly with grand jury and False Claims Act matters. He also counsels pharmaceutical and medical device companies regarding regulatory reporting and submission requirements, GMP/QSR and marketing matters.
|Date:||June 22 – July 17, 2009|
|Location:||Your office or conference room (no need to travel!)|
Gather your team for maximum benefit! Your investment is for one dial-in.
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