Strategies for Preparing and Submitting Successful Citizen Petitions and Suitability Petitions to FDA

This 90-minute webinar will recommend strategies for filing successful Citizen Petitions and Suitability Petitions with the U.S. Food and Drug Administration. You will learn techniques for drafting and filing successful petitions including the required elements of such petitions and the types of substantiation needed to support them.

Why Should You Attend:

The webinar is intended to provide participants with strategies for drafting targeted and effective Citizen Petitions and Suitability Petitions for submission to FDA. Recommendations for strengthening petitions and increasing the chances of ultimate success will also be provided.

Who Will Benefit:

- In-House Counsel, General Counsel, Asst. General Counsel, members of a company's Regulatory Affairs and Legal departments; and members of the branded pharmaceutical and generic drug industries generally.
- Managers, Consultants, Scientists, Research Analysts, State Policy Officials
- Investment Analysts, Venture Capitalists, Financial analysts, investors watching the pharmaceutical, life sciences and biotech industries

Event Details:
Date: August 28, 2012
Time: 10:00 AM - 11:30 AM PDT
Cost: $349 per attendee per computer terminal
Registration: SIgn-Up on-line now. Add to your shopping cart.

Karl Nobert, is a food and drug regulatory attorney with the law firm of Squire Sanders in Washington, DC. He frequently assists clients with the development and execution of regulatory strategies for supporting the product life cycle and expediting the approval process via the use of Citizen Petitions and Suitability Petitions.

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