|Quantity Discounts||1 - 9999|
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And the stakes keep growing. Did you know ... warning letters due to clinical trial problems more than doubled from 2006 to 2009.
Stronger agreements are the answer. You need a lawyer’s advice ... without paying a lawyer’s fee. FDAnews has invited a leading litigator, Chris Johnson of Shook Hardy & Bacon, to help you bulletproof your international clinical trial agreements.
Without leaving your desk, you’ll learn the basics of drafting clinical trial agreements, international and domestic. You’ll cover key elements of ironclad agreements ... hear tips to mitigate risks ... review case studies of recent litigations ... get checklists for creating agreements ... and take away sample agreements to study at your leisure. Presentation specifics include:
It’s 90 nonstop minutes of interactive learning. And because the session takes place via the web, you’ll have every opportunity to get answers to questions you email the presenter.
Make sure everyone in your company is on hand who deals with international clinical trials. There’s no limit on number of participants at one location; the price is the same regardless of how many log on.
Stop worrying whether the FDA or some overseas regulator will block your trials. Properly drafted CTAs are the answer to regulatory hurdles and lawsuits, and the path to greater clinical-trial success. Can you afford not to sign up?
Chris Johnson is a partner in the San Francisco office of Shook Hardy & Bacon, specializing in medical, scientific and statistical defense strategies in complex civil litigations. International clinical trials are a focus of his work. He has assembled an in-house team of allied medical and scientific professionals to conduct medical case review and research.
|Date:||Nov. 2–20, 2009|
|Location:||Your office or conference room (no need to travel!)|
Gather your team for maximum benefit! Your investment is for one dial-in.
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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