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Drafting the Scope Drafting the Scope
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The Structure of the Patent Specification The Structure of the Patent Specification
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Priority and Foreign Filing Texts Priority and Foreign Filing Texts
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Background of the Invention and Prior Art Background of the Invention and Prior Art
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The European Patent Office: Problem and Solution The European Patent Office: Problem and Solution
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The United States: Danger of Estoppel The United States: Danger of Estoppel
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Selection Inventions Selection Inventions
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Addition of Reference to Prior Art Addition of Reference to Prior Art
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Object of the Invention Object of the Invention
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United States Sufficiency Requirements United States Sufficiency Requirements
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Written Description Written Description
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How to Make How to Make
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How to Use How to Use
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Best Mode Best Mode
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Sufficiency Requirements in the United Kingdom and the European Patent Office Sufficiency Requirements in the United Kingdom and the European Patent Office
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Sufficiency Requirements in Other Countries Sufficiency Requirements in Other Countries
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Special Requirements for Biotech Inventions Special Requirements for Biotech Inventions
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Microbiological Inventions Microbiological Inventions
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Inventions Involving DNA Sequences Inventions Involving DNA Sequences
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Length of Text Length of Text
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General Rule General Rule
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Incorporation by Reference Incorporation by Reference
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17 Drafting the Patent Specification
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Published:December 2016
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Abstract
This chapter explains the procedure for drafting a patent specification. When an invention of any kind has been made, the first step towards drafting a patent specification is defining the scope of the invention, or forming a mental picture of what is to be claimed. The second step is putting that mental picture into words. Once the patent attorney gains a clear picture of the correct scope of the invention, he or she can begin the task of drafting the specification and claims of the application. The remainder of the chapter discusses the structure of the patent specification; priority and foreign filing texts; sufficient requirements in the US, UK, and other countries; and special requirements for biotech inventions.
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