Intellectual property (IP) is a valuable asset to companies in the biotech, life sciences, healthcare, medical technology and related industries. Utility patents are often the most valuable IP belonging to small and emerging companies.
Intellectual Property includes patents, trademarks, service marks, copyrights, and trade secrets. This value-added asset can be sold, bought and traded as a part of everyday commerce.
It is important for a company to know what IP it has and how to enhance the company's IP position which, in turn, enhances the company's valuation.
Patents are often the most valuable IP asset for most companies. Strictly speaking there are three types of U.S. patents:
(1) Design Patents (for example, an ornamental design for an article of manufacture)
"Whoever invents or discovers any new and useful process, machine, manufacture, or composition of matter, or any new and useful improvement thereof, may obtain a patent therefore, subject to the conditions and requirements of this title." (35 U.S.C., §101)
Equally as important as what is patentable is what is not patentable. What are not patentable are:
(1) Laws of nature
However, what constitutes patentable subject matter has come under broad interpretation as a result of the U.S. Supreme Court decision in Diamond vs. Chakraborty (1980), which established that companies or individuals could receive utility patents for newly created organisms. Since then, the biotechnology industry has argued that patents should issue on genes, proteins and other natural materials which have commercial value.
Primarily as an effort to boost U.S. eminence and competitiveness to the then fledgling but growing biotech industry, shortly after the Diamond vs. Chakraborty decision the U.S. Patent Office (USPTO) began issuing patents on products of nature including genes (human or otherwise), gene fragments, cell lines, proteins and other naturally occurring substances.
As a result of increasingly growing criticism, the USPTO has recently issued utility patent guidelines and rules regarding a stricter definition of what is invented or patentable. These new guidelines and rules call for utility patents to have "specific and substantial utility that is credible."
No longer will it be sufficient to claim that a particular biological or molecular probe (DNA, protein, etc.) to be a useful probe, the new utility test calls for specific utility regarding that particular molecular probe (i.e., a probe for a particular gene, a probe for a specific disease state or a probe for a defined location on a chromosome).
In addition, it is no longer acceptable to make general claims regarding utility and usefulness. For example, it will not be acceptable to claim that a protein is a source of amino acids or a feed supplement or a dietary supplement, but real-world utility must be specified and demonstrated.
The new utility patent guidelines and rules will have a profound effect on the biotech and related industries.
Visit www.BusinessOfScience.com for additional information concerning Intellectual Property and the business of science and technology.
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ABOUT THE AUTHOR
Louis M. Scarmoutzos, Ph.D., or "Dr. Lou" as his colleagues and friends fondly call him, is President & Founder of MVS Solutions, Inc., a corporate and technology development company focused on the biotech, chemistry, pharma, medical and related industries.
Dr. Scarmoutzos received his B.S. cum laude in Chemistry from Boston College, a Ph.D. summa cum laude in Physical Organic Chemistry from the Pennsylvania State University and was a Post-Doctoral Fellow in the Department of Chemistry and Chemical Biology at Harvard University. Dr. Scarmoutzos serves as a Principal Advisor to the Los Angeles Research and Technology Association (Larta) Life Sciences Technology Group and a Principal Advisor in the National Institutes of Health Commercialization Assistance Program (NIH-CAP). Additional info about Dr. Scarmoutzos and MVS Solutions may be found at www.mvssolutions.com