Articles
Published on 16 December 2016
Data requirements to demonstrate biosimilarity in the EU
Author(s): GaBI Journal Editor
biosimilar, biosimiliarity, data requirements, extrapolation
DOI: 10.5639/gabij.2016.0504.047
6.907 views
Editor's Letter
Published on 16 December 2016
Fourth and final issue of GaBI Journal’s fifth volume
Author(s): Professor Philip D Walson, MD
DOI: 10.5639/gabij.2016.0504.038
3.869 views
Published on 14 December 2016
Biosimilar product labels in Europe: what information should they contain?
Author(s): GaBI Journal Editor
biosimilar, labelling, patients, pharmacists, physicians, Summary of Product Characteristics (SmPC)
DOI: 10.5639/gabij.2017.0601.008
9.663 views
Published on 14 December 2016
Overview of the patent expiry of (non-)tyrosine kinase inhibitors approved for clinical use in the EU and the US
Author(s): Associate Professor Martine Lamfers, PhD, Professor Arnold G Vulto, PharmD, PhD, FCP, Professor Sieger Leenstra, MD, PhD, Subramanian Venkatesan, MSc
anticancer drugs, kinase inhibitors, market exclusivity, patent expiry, targeted therapies
DOI: 10.5639/gabij.2017.0602.016
61.999 views
Published on 14 December 2016
Pharmacovigilance of biosimilars and other biologicals within the hospital: current practices and future challenges
Author(s): Barbara OM Claus, PharmD, PhD, Professor Annemie Somers, PharmD, PhD, Tiene Bauters, PharmD, PhD
biologicals, biosimilars, hospitals, pharmacovigilance
DOI: 10.5639/gabij.2017.0601.005
8.283 views
Published on 14 December 2016
Naming and labelling of biologicals – a survey of US physicians’ perspectives
Author(s): Harry L Gewanter, MD, FAAP, FACR, Michael S Reilly, Esq
ASBM, biosimilar, interchangeability, labelling, legislation, naming
DOI: 10.5639/gabij.2017.0601.003
10.592 views
Published on 14 December 2016
An empirical study of market-based purchasing policies for generic pharmaceuticals in Sweden
Author(s): GaBI Journal Editor
DOI: 10.5639/gabij.2016.0504.050
4.157 views
Published on 12 December 2016
The role of European Pharmacopoeia monographs in setting quality standards for biotherapeutic products
Author(s): Emmanuelle Charton, PhD
biotherapeutic products, complexity of biologicals, monographs, pharmacopoeia, public standards
DOI: 10.5639/gabij.2016.0504.045
21.007 views
Published on 12 December 2016
Strategies used to delay or prevent access to affordable generic drugs in the US
Author(s): GaBI Journal Editor
DOI: 10.5639/gabij.2016.0504.051
5.142 views
Published on 31 October 2016
Essential information for internists on biologicals and biosimilars
Author(s): GaBI Journal Editor
DOI: 10.5639/gabij.2016.0504.049
4.176 views
Published on 31 October 2016
Effect of naming on pharmacists’ perceptions and dispensing of biosimilars
Author(s): GaBI Journal Editor
DOI: 10.5639/gabij.2016.0504.048
7.080 views