Amendments to the requirements for brandname-drug patents have been proposed by the US FDA

Author：  

Publisher： Adis International

ISSN： 1173-8324

Source： Inpharma, Vol.1, Iss.1368, 2002-01, pp. : 3-3

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

The endpoints used by the US FDA to approve new oncology drug applications have been summarised

By  

Inpharma, Vol. 1, Iss. 1387, 2003-01 ,pp. : 4-4

Adis International

Access to resources Recommend Favorite

Guidelines for the sale of dietary supplements have been relaxed by the US FDA

By  

Inpharma, Vol. 1, Iss. 1222, 2000-01 ,pp. : 2-2

Adis International

Access to resources Recommend Favorite

New legislation aimed at severing the close ties between the US FDA and drug companies has been introduced in the US.

By  

Inpharma, Vol. 1, Iss. 1488, 2005-01 ,pp. : 21-21

Adis International

Access to resources Recommend Favorite

Astellas Pharma's Supplemental New Drug Application (sNDA) for injectable micafungin [Mycamine] has been approved by the US FDA.

By  

Inpharma, Vol. 1, Iss. 1623, 2008-01 ,pp. : 18-18

Adis International

Access to resources Recommend Favorite

The US Congress has passed the FDA Amendments Act of 2007

By  

Reactions Weekly, Vol. 1, Iss. 1171, 2007-01 ,pp. : 3-3

Adis International

Access to resources Recommend Favorite