Policies & Legislation

New Zealand to fund only biosimilar epoetin alfa

Home/Policies & Legislation | Posted 09/11/2018

New Zealand will stop funding the brand-name epoetin alfa biological Eprex and, in future, will only fund the biosimilar epoetin alfa Binocrit.

EU-US mutual recognition extended to include Portugal

Home/Policies & Legislation | Posted 02/11/2018

The European Medicines Agency (EMA) announced on 20 September 2018 that the Mutual Recognition Agreement between the European Union and the US had been extended to include one additional EU Member State, Portugal.

Australia encouraging biosimilars and mandating drug shortage reporting

Home/Policies & Legislation | Posted 19/10/2018

In an effort to address both the rising prices of medicines and the risk of drug shortages in Australia the country has introduced drivers to encourage the use of biosimilars and mandatory reporting of drug shortages.

EMA aims to improve the availability of medicines in Europe

Home/Policies & Legislation | Posted 12/10/2018

A European Union (EU) task force, which was set up by European regulators, has published its work programme for 2019/20 and announces a multi-stakeholder workshop.

Biosimilars no longer eligible for parallel processing in Australia

Home/Policies & Legislation | Posted 05/10/2018

Biosimilars will no longer be able to request parallel processing when submitting a biosimilar application for approval in Australia.

Mexico trade deal impacts biologicals exclusivity

Home/Policies & Legislation | Posted 21/09/2018

The US announced a new ‘understanding’ on trade with Mexico on 27 August 2018.  The announcement comes as part of efforts to re-negotiate the North American Free Trade Agreement (NAFTA) between the US, Canada and Mexico, which first came into force in January 1994.

AbbVie ruled to pay nearly US$450 million for antitrust violations

Home/Policies & Legislation | Posted 14/09/2018

AbbVie and their partner firm Besins Healthcare have been ordered by the Federal Trade Commission (FTC) to pay US$448 million for preventing generics competition to their testosterone product Androgel. This is the largest amount ever seen in an FTC antitrust case.

EU reinforces collaborations with US and Japan

Home/Policies & Legislation | Posted 31/08/2018

The European Union (EU) is reinforcing its collaborations with both the US and Japan.

Russian court approves first compulsory licence

Home/Policies & Legislation | Posted 20/07/2018

A court in Moscow has made history by granting a compulsory licence to Russian drugmaker Ukrenergo to make a generic version of Celgene Corporation’s (Celgene) flagship blood cancer drug Revlimid (lenalidomide).

CFDA to come under national market supervision administration

Home/Policies & Legislation | Posted 20/04/2018

A sweeping government restructuring plan was approved by China’s National People’s Congress on 17 March 2018. The reorganization will see China’s drug regulator, the China Food and Drug Administration (CFDA), merged into an overarching market supervision administration.