2016/3 GaBI Journal Table of Contents

Published in: Volume 5 / Year 2016 / Issue 3
Category: 2016/3 GaBI Journal Table of Contents
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Contents

Editor’s Letter

Latest features in GaBI Journal, 2016, Issue 3

Letters to the Editor

Is the EU ready for non-biological complex drug products?

Commentary

Biosimilars: achieving long-term savings and competitive markets

Review Article

Current state of subsequent entry biologics (biosimilars) in Canada: a view from regulatory, reimbursement, clinician, and patient perspectives

The generic medicines system in Italy: scenarios for sustainable growth

Perspective

Pharmacovigilance on biologicals and biosimilars: a Danish perspective

Regional management of biosimilars in Germany

Are the perspectives regarding the use of biosimilars in the setting of haematology and blood and marrow transplant changing?

Biosimilars in Italy: a gastroenterologist’s view

Meeting Report

First Turkish interactive workshop on regulation and approval of similar biotherapeutic products/biosimilars, 2–3 March 2016, Ankara, Turkey

Demonstrating interchangeability and biosimilarity for US biosimilars

Special Report

US FDA proposals for naming of biologicals and labelling of biosimilars

Competitive effects on the generics industry

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