From Clones to Claims
A Handbook on Patenting Biotech and Biopharmaceutical Inventions in the European Patent Office
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»From Clones to Claims« has evolved as a reaction to the ready internet availability of all decisions of the Boards of Appeal of the European Patent Office (EPO). While the increased availability is one thing, using the information in daily practice is another. This translation is the aim of the 7th edition of this book. It has become a guide through the available decisions not only of Boards 3.3.04 and 3.3.08 the initial biotech Boards but also of Boards 3.3.01 and 3.3.02, which have meanwhile also begun to hear biotech cases. This reflects the overwhelming development and expansion of biot...
»From Clones to Claims« has evolved as a reaction to the ready internet availability of all decisions of the Boards of Appeal of the European Patent Office (EPO). While the increased availability is one thing, using the information in daily practice is another. This translation is the aim of the 7th edition of this book. It has become a guide through the available decisions not only of Boards 3.3.04 and 3.3.08 the initial biotech Boards but also of Boards 3.3.01 and 3.3.02, which have meanwhile also begun to hear biotech cases. This reflects the overwhelming development and expansion of biotech into the field of biopharmaceuticals, for example, the advent of antibody drugs against several types of life-threatening cancer and chronic diseases, such as rheumatoid arthritis. One of the best current examples of the importance of biopharmaceuticals was the virtually immediate advent of powerful vaccines against the causative agent of the corona (SARS-CoV-2/Covid-19) pandemic. »From Clones to Claims« contains extra chapters on the patenting of viruses and related vaccines. This is just one example of the chapters in the expanded version. This 7th edition also contains other supplemental chapters in view of recent developments in science and related jurisprudence. For example, new or substantially revised chapters include a new, more elaborate chapter on SPCs; a new chapter on plausibility, with express consideration of pending case G 2/21; as well as new chapters on next generation sequencing technologies and personalized medicines/companion diagnostics. A further new chapter addresses CRISPR, outlining and discussing the complex pattern of oppositions and appeals in the EPO concerning this revolutionary, Nobel prize winning technology. Thus, the current jurisprudence of the Boards of Appeal of the EPO is systematically organized according to the following topics:
Products of Nature: What is Patentable in the EPO (compounds, stem cells, plants, etc.)The Person Skilled in the ArtThe Principles Applied by the Technical Boards in Assessing the Disclosure of a Document and their ImplicationsThe Principles Applied by the Technical Boards in Claim ConstructionPlausibility as a Means to Assess Quid Pro QuoThe Principles of Patenting Medical and Diagnostic UsesPatenting Nucleic Acid InventionsPatenting Protein InventionsPatenting Antibody InventionsPatenting Microorganisms and Fermentation TechnologiesPatenting VirusesPatenting Stem Cells and Cell-based TherapeuticsPatenting Nucleic Acid Amplification TechnologiesPatenting Nucleic Acid Modification Technologies: CRISPR et al.Patenting Next Generation Sequencing TechnologiesPatenting Personalized Medicines and Companion DiagnosticsPatenting Plants and AnimalsPriority Hurdles of Same Subject Matter and Legal EntitlementDepositHow to draft a European Patent Application and ClaimsA Brief Introduction to the Extension of Patent Terms
As is evident, this expanded version of »From Clones to Claims« solely focuses on EPO Appeal Board jurisprudence and SPCs. It no longer addresses jurisprudence from the US or Japan as a consequence of the technically limited space in such a product. Thus, the new version is a detailed guide on how to prepare European patent applications in any particular field of biopharmaceuticals and how to best defend the European patents once granted. Given this, the book is not only useful for advanced practitioners, but also for beginners as an introduction into and an orientation to the field of biotechnology patents.
Given the book's clear language and systematic structure, the EPO's jurisprudence is
Products of Nature: What is Patentable in the EPO (compounds, stem cells, plants, etc.)The Person Skilled in the ArtThe Principles Applied by the Technical Boards in Assessing the Disclosure of a Document and their ImplicationsThe Principles Applied by the Technical Boards in Claim ConstructionPlausibility as a Means to Assess Quid Pro QuoThe Principles of Patenting Medical and Diagnostic UsesPatenting Nucleic Acid InventionsPatenting Protein InventionsPatenting Antibody InventionsPatenting Microorganisms and Fermentation TechnologiesPatenting VirusesPatenting Stem Cells and Cell-based TherapeuticsPatenting Nucleic Acid Amplification TechnologiesPatenting Nucleic Acid Modification Technologies: CRISPR et al.Patenting Next Generation Sequencing TechnologiesPatenting Personalized Medicines and Companion DiagnosticsPatenting Plants and AnimalsPriority Hurdles of Same Subject Matter and Legal EntitlementDepositHow to draft a European Patent Application and ClaimsA Brief Introduction to the Extension of Patent Terms
As is evident, this expanded version of »From Clones to Claims« solely focuses on EPO Appeal Board jurisprudence and SPCs. It no longer addresses jurisprudence from the US or Japan as a consequence of the technically limited space in such a product. Thus, the new version is a detailed guide on how to prepare European patent applications in any particular field of biopharmaceuticals and how to best defend the European patents once granted. Given this, the book is not only useful for advanced practitioners, but also for beginners as an introduction into and an orientation to the field of biotechnology patents.
Given the book's clear language and systematic structure, the EPO's jurisprudence is
