3rd AnnualHatch-Waxman Boot CampA Primer on IP Basics and Regulatory Fundamentals Relative to Small Molecules and BiologicsMonday, June 25 to Tuesday, June 26, 2012
Hilton San Diego Resort & Spa, San Diego, CA
ACI, the nation’s premier provider of life sciences intellectual property conferences, is pleased to bring the third west coast installment of its renowned Hatch-Waxman Series back to San Diego. 2011 brought the enactment of the America Invents Act and 2012 marked the release of the FDA Draft Guidance on Biosimilars. Understand how this will impact the Hatch-Waxman arena. Now in its third year, Hatch-Waxman Boot Camp – San Diego Edition has become the gathering place of the Southern California life sciences IP Bar. With the precedential regulatory changes in the IP regulatory arena there will clearly be impacts to Hatch-Waxman. Attend this essential event to understand the interplay of IP and FDA regulation relative to pharma/biotech patents vis-à-vis Hatch-Waxman and recently released biosimilars guidance and ensure that you are aware of the intersection of the newly promulgated America Invents Act with Hatch-Waxman. It is vital to understand how all these components work together and that both will influence the Hatch-Waxman rubric. A thorough understanding of Hatch-Waxman is absolutely essential to anyone working in the biopharmaceutical area. This knowledge sets the foundation for the protection of small molecules and small proteins and provides the tools to ponder an IP and regulatory framework for what lies beyond the realm of traditional pharmaceuticals. The highly regulated nature of the products which the pharmaceutical and biotechnology industries manufacture dictates that the patenting of these products be closely tied to regulatory approval by the FDA. Anyone who works in the life sciences industry – and who even remotely deals with its IP – must be well versed in the regulatory components and IP subtleties that play such an integral role in the patenting of its products. You cannot afford to be left in the dark regarding the interconnection of IP and FDA regulation in these industries. Gain the competitive edge – boost your life sciences IP and regulatory IQ. ACI’s Hatch-Waxman Boot Camp has been designed to give counsel and advisors to brand name and generic drug companies and biopharmas – critical insights into commercialization and the pre-approval process, and also provide you an in-depth review of Hatch-Waxman and other IP basics relative to small molecules and biologics. This conference will lay the necessary foundation for you to thoroughly comprehend the dynamics of the applicable patent life cycles for pharmaceutical and biopharmaceutical products and business development plans. Master the intricacies of the patent and regulatory framework for drugs and biologics. A faculty of top-notch IP and regulatory counsel all having a wealth of experience through working for brand names and generics as well as biopharmas – will share their knowledge on:
Also, in response to your requests, we have added a special Interactive Biosimilars Strategy Session, which will provide an overview of the law governing biosimilars and will then delve into interactive hypotheticals about the inner-workings of the BPCIA and anticipated litigation scenarios.New for 2012 is a post-conference workshop Patent Reform 101: Overview of the Fundamental Provisions in the America Invents Act and the Impact on Hatch-Waxman Litigation, which will walk you through the AIA and highlight important aspects of the Act vis-à-vis Hatch-Waxman, including understanding the implementation schedule for certain provisions of the Act.Attend this conference and learn to navigate your way through the IP and regulatory mazes that play such a crucial role in your practice areas. Register now by calling 1-888-224-2480, faxing your registration form to 1-877-927-1563, or registering online at www.AmericanConference.com/HWBootCamp |
Brochure
![]() - click image for pdf - Dates: Mon, Jun 25, 2012 Tue, Jun 26, 2012 Location:
Accreditation:Hilton San Diego Resort & Spa San Diego, CA Accreditation will be sought in those jurisdictions requested by the registrants which have continuing education requirements. This course is identified as nontransitional for the purposes of CLE accreditation. ACI certifies that the activity has been approved for CLE credit by the New York State Continuing Legal Education Board in the amount of 15.0 hours. An additional 3.5 credit hours will apply to each workshop. ACI certifies that this activity has been approved for CLE credit by the State Bar of California in the amount of 12.5 hours. An additional 3.0 credit hours will apply to each workshop.You are required to bring your state bar number to complete the appropriate state forms during the conference. CLE credits are processed in 4-8 weeks after a conference is held. ACI has a dedicated team which processes requests for state approval. Please note that event accreditation varies by state and ACI will make every effort to process your request.Questions about CLE credits for your state? Visit our online CLE Help Center at www.americanconference.com/CLE |
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