Buch, Englisch, 63 Seiten, broschiert, Format (B × H): 153 mm x 227 mm, Gewicht: 137 g
Reihe: MIPLC studies
Buch, Englisch, 63 Seiten, broschiert, Format (B × H): 153 mm x 227 mm, Gewicht: 137 g
Reihe: MIPLC studies
ISBN: 978-3-8487-5221-8
Verlag: Nomos
FTO licensing in the pharmaceutical industry deserves special consideration because of the large economic scale of the market, expensive cost of R&D, extremely low success rate, and easy duplication of the drug. Taking these unique aspects into consideration, the author first explaines how to perform a good FTO search and conclude an appropriate FTO licensing agreement, and then points out two issues; (i) the issue of FTO licensing and EU competition, especially the unreasonable application of the Guideline, and (ii) the issue of FTO licensing and differentiating between a bio venture company and a pharmaceutical company. Solutions for these issues are proposed.
The author is Hirotaka Nonaka; an attorney-at-law and patent attorney in Tokyo, Japan, handling particularly IP-related disputes and consulting.
