Further capping of generics in Japan

Home/Policies & Legislation | Posted 29/01/2016 post-comment0 Post your comment

In a bid to increase uptake of more cost-effective drugs and to curb healthcare spending, the Japanese Government has put forward plans to price generics at half the cost of brand-name drugs from April 2016, a reduction of 10%.

pill bottles V14K20

This initiative comes as an attempt to reduce drug costs in Japan, which have been found to be much greater than the average of industrialized nations [1].

As part of the government’s proposals, pharmaceutical companies will be allowed to sell a generic version of a brand-name drug after patent expiration if the quality of the generic drug is deemed to be on a par with the brand-name version. This will be priced lower than its brand-name counterpart owing to the lower research and developmental costs.

Generics of brand-name drugs manufactured by different companies will be priced at 40% of the originator drugs and biotechnology-based biosimilars will be priced initially at 70%.

The government is also expected to limit fees to hospitals and doctors, saving them an estimated US$3.5 billion.

This follows a target already set of 80% for generics prescribing by March 2021. It currently stands at 50% but is expected to reach 70% in 2017. The drive to reduce healthcare spend comes against the backdrop of an ageing population in Japan that is requiring increased medical care.

Related article
Europe–Japan cooperation on generics and biosimilars regulation 

Reference
1.  GaBI Online - Generics and Biosimilars Initiative. Prescribing and dispensing generics in Japan [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2016 Jan 29]. Available from: www.gabionline.net/Generics/Research/Prescribing-and-dispensing-generics-in-Japan  

Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.

Copyright – Unless otherwise stated all contents of this website are © 2016 Pro Pharma Communications International. All Rights Reserved.

Source: Japan Times

comment icon Comments (0)
Post your comment
Related content
NPRA Malaysia trials new timelines for variation applications
24-AA011041
Home/Policies & Legislation Posted 05/11/2024
China’s NMPA expands global ties with the Netherlands and Indonesia
China CFDA NMPA
Home/Policies & Legislation Posted 04/09/2024
Japan's PMDA expands influence with new office in Thailand
Conference V14A17
Home/Policies & Legislation Posted 06/08/2024
Most viewed articles
About GaBI
Home/About GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
Home/Guidelines Posted 08/10/2010