Instructor:
Charlie Sodano
Product ID: 702496
Why Should You Attend:
The process of obtaining patents can be an involved, expensive and specialized process although the USPTO and other governmental agencies have in recent years tried to simplify the process and promote electronic submission.
The documentation requirements for research supporting to the granting of a patent is changing. The “first to invent” will no longer be the one to get the patent. It increasingly concerns proper control of records that corroborate the invention and distinguish it from prior public disclosures.
This webinar will help you establish a system that will minimize problems in filing and defending patents.
Areas Covered in the Webinar:
Who Will Benefit:
Dr. Charlie Sodano, is an experienced, globally recognized information management professional. He began his career as a discovery research chemist at Pfizer and since 1985 has specialized in the management of electronic as well as paper based records and information. He managed Information Services departments at RJR Nabisco, Berlex Biosciences and Bayer HealthCare Pharmaceuticals and holds BS and MS and Ph.D. degrees in Chemistry. In December, 2007 he launched eOrganizedWorld a consulting firm specializing in the planning and implementation of records and information management systems.
Topic Background:
On September 16, 2011, President Obama signed the Leahy-Smith America Invents Act into law. Several important changes took effect on the date of enactment, including some significant litigation related changes and the new standard for instituting reexamination. Most other changes take effect in one year, although the changes to the definition of prior art (including the "first-to-file" provisions) and new post-grant review proceedings will not take effect for 18 months.
Research records that are used to support patent claims must meet stringent requirements to be viable in support of patent applications and in case of litigation. They must be authenticated records that support:
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