Pharmaceutical Patents under the SPC Regulation

Pharmaceutical Patents under the SPC Regulation

Callesen Klinge, Ulla

Edward Elgar Publishing Ltd

10/2022

286

Dura

Inglês

9781803927374

15 a 20 dias

Descrição não disponível.
Contents: Preface PART I INTRODUCTION AND CONTEXT 1. Introduction to Pharmaceutical Patents under the SPC Regulation 2. The Pharmaceutical Industry and the Surrounding Legal and Economic Environment PART II LEGAL ANALYSIS OF THE SPC REGULATION AS IT IS 3. Background and Purpose of the SPC System 4. Definition of "Product" and "Medicinal Product" 5. Eligibility for Protection of (Medicinal) Products under the SPC System 6. Conditions for Obtaining a Certificate (Art. 3) 7. Subject Matter of Protection (Art. 4) and Effects of the Certificate (Art. 5) 8. Conclusion on the Law as it is PART III LEGAL ANALYSIS OF THE SPC REGULATION WITH REGARD TO MODERN PHARMACEUTICAL INNOVATION 9. SPC protection for biotechnological medicinal products 10. Secondary innovation PART IV GENERAL FINDINGS AND FUTURE PROPOSALS 11. General Findings and Future Proposals Bibliography Index
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SPC, supplementary protection certificate, case law, technological/pharmaceutical development, biopharmaceuticals, scope of protection