Chinas guidebook for pharmaceutical patent protection
Aarkstore.com announces, The Latest market research report is available inits vast collection:Chinas Guidebook for Pharmaceutical Patent ProtectionYou can also request for sample page of above mention reports firstname.lastname@example.orgChina is expected to become the fifth largest drug market in the world by 2010 witha growth rate of 20-25 percent per annum in next three years. As China joins theWorld Trade Organization (WTO) and integrates more completely into the globaleconomy, it will further open the door to a lucrative drug market for overseaspharmaceutical companies, which attracts more and more overseas pharmaceuticalmanufacturers and producers to enter such drug market and seize a larger part ofsuch drug market. However, the Chinese social environment for the protection ofintellectual property right is complex. The locally produced generics and copyproducts dominate the Chinese drug market. It is estimated that about 97 percent ofthe drugs produced by local companies are generics or counterfeitsGuidebook Highlights: China’s Guidebook for Pharmaceutical Patent Protection provides a comprehensiveand thorough knowledge of the Chinese patent system relating to pharmaceuticals,the detailed administrative, civil and criminal judicial pathways for protections ofpatent right, and the design for composition of optimized protection strategies.
The organization structure of patent authorities and judicial system; A comprehensive and thorough knowledge of the Chinese patent system and therelevant laws and administrative regulations relating to pharmaceuticals;Table of contents:Preface 6Chapter 1. Introduction 9Chapter 2 . Organization Structure of Patent Authorities and JudicialSystem 122.1. Organization Structure of Patent Authorities 122.2. Organization Structure of Judicial System 142.3. Responsibilities of the State Intellectual Property Office (SIPO) 152.3.1. Responsibilities of the Patent Office 152.3.2. Responsibilities of the Patent Reexamination Board 16Chapter 3. The Objects of Patent Right 173.1. The Objects of Patent Right 173.2. The Non-Patentable Subject Matter 18Chapter 4. The Patentable Subject Matter Relating to Pharmaceuticals 194.1. The Patentable Subject Matters for Invention 194.2. The Patentable Subject Matters for Utility Model 224.3. The Patentable Subject Matters for Design 22Chapter 5. Application for Patent 235.1. The Right of Patent Application 235.2. The Applicant for Patent 245.3.1. The Date of Filing 255.3.2. The Priority Date 255.4. Application for Patent 275.4.1. Application for a Patent for Invention or Utility Model 285.4.2. Application for a Patent for Design 33List of FiguresList of Tables are also include.
For more Reports Plz follow The link:Material and Clinical Trial Requirements of Application and Approval for ImportedDrug Registration: A Guidebook of Registration Application.... China PharmaceuticalGuidebook Series (3)(4th edition)Material and Clinical Trial Requirements of Application and Approval for ImportedDrug Registration: A Guidebook of Registration Application for Imported BiologicalProducts China Pharmaceutical Guidebook Series (4) (4th edition)Invest in China: A Guidebook for Application and Approval of EstablishmentRegistration for Foreign Investment Enterprises(The Invest in China GuidebookSeries (1)China Pharmaceutical Guidebook: Latest Chinese Regulations for Imported DrugRegistration(4th Edition)Chinas Guidebook for Pharmaceutical Patent ProtectionSearch More Reports Related to This Category :Chinas Guidebookhttp://www.aarkstore.com/search/viewresults.asp?search=Guidebook&PubId=&pagenum=1For More details Plz do contact :Aarkstore EnterpriseLavanyaPhone:08149852585