This article examines the development of mutual recognition of marketing authorizations for pharmaceuticals, arguing that the sui generis approach to mutual recognition in this policy area is based, first of all, on the harmonisation of regulatory requirements. However, it additionally also required the procedural integration of mutual recognition in trans-national administrative procedures, and institutional innovation. This has created a curious mix of centralized and decentralized authorisation routes with various stages of collaboration and arbitration. In this regard, the creation of the complex, composite procedures in place to facilitate the mutual recognition of pharmaceuticals raises several questions with regard to the judicial an...
Ensuring universal access to medicines is an important topic of the international agenda and nationa...
'The EC harmonized market entry regulation for pharmaceuticals from the early sixties on, but it ach...
Background: In the European Union (EU), a medicinal product needs a marketing authorization (MA) to ...
This article examines the development of mutual recognition of marketing authorizations for pharmace...
In the EU, pharmaceuticals are subject to a marketing authorisation requirement that, depending on t...
In the EU, pharmaceuticals are subject to a marketing authorisation requirement that, depending on t...
This article analyses the setting of global pharmaceutical standards in the International Council fo...
Historically drug regulation has been virtually synonymous with national sovereignty. Over the last ...
This article deals with mutual recognition in relation to the free movement of goods and aims to dem...
Abstract Background As a transnational policy network, the International Council for Harmonization o...
"The EC harmonized market entry regulation for pharmaceuticals from the early sixties on, but it ach...
The EC harmonized market entry regulation for pharmaceuticals from the early sixties on, but it achi...
This book analyses the implementation of global pharmaceutical impact standards in the European risk...
Mutual recognition is generally not mentioned in debates about new modes of governance, though it is...
Ensuring universal access to medicines is an important topic of the international agenda and nationa...
'The EC harmonized market entry regulation for pharmaceuticals from the early sixties on, but it ach...
Background: In the European Union (EU), a medicinal product needs a marketing authorization (MA) to ...
This article examines the development of mutual recognition of marketing authorizations for pharmace...
In the EU, pharmaceuticals are subject to a marketing authorisation requirement that, depending on t...
In the EU, pharmaceuticals are subject to a marketing authorisation requirement that, depending on t...
This article analyses the setting of global pharmaceutical standards in the International Council fo...
Historically drug regulation has been virtually synonymous with national sovereignty. Over the last ...
This article deals with mutual recognition in relation to the free movement of goods and aims to dem...
Abstract Background As a transnational policy network, the International Council for Harmonization o...
"The EC harmonized market entry regulation for pharmaceuticals from the early sixties on, but it ach...
The EC harmonized market entry regulation for pharmaceuticals from the early sixties on, but it achi...
This book analyses the implementation of global pharmaceutical impact standards in the European risk...
Mutual recognition is generally not mentioned in debates about new modes of governance, though it is...
Ensuring universal access to medicines is an important topic of the international agenda and nationa...
'The EC harmonized market entry regulation for pharmaceuticals from the early sixties on, but it ach...
Background: In the European Union (EU), a medicinal product needs a marketing authorization (MA) to ...