Patentability of Pharmaceutical Dosage Regimens in Europe

Akin to other inventions, new methods need to be devised allowing forregistration of pharmaceutical dosage regimens in much the same way asother patents. In doing so, there are two main challenges ahead. First,whether these dosage regimens, excluded expressly from the list ofpatentable products in E...

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Bibliographic Details
Main Authors: Mahdi Zahedi, Mohammad Hosein Erfanmanesh
Format: Article
Language:fas
Published: Allameh Tabataba'i University Press 2013-03-01
Series:Faṣlnāmah-i Pizhūhish-i Huqūq-i Khuṣūṣī
Subjects:
Online Access:https://jplr.atu.ac.ir/article_2240_5420911b468e9f922e2fea305fcfa6ad.pdf
Description
Summary:Akin to other inventions, new methods need to be devised allowing forregistration of pharmaceutical dosage regimens in much the same way asother patents. In doing so, there are two main challenges ahead. First,whether these dosage regimens, excluded expressly from the list ofpatentable products in Europe, may in fact be considered as a novel therapymethod? And second, given that ingredients and composition of such patentsare no longer an innovative secret, whether sole variation in their usagedosage may possibly fall within the scope of novel inventions?The answer to the above controversial questions have been the notion ofchallenge addressed by several European patent forums. This article willreview the approaches adopted by European Patent Administration indealing with recent trends introduced on the topic of new customized dosageregimens
ISSN:2345-3583
2476-6232