Opinion
Tell me the whole story: the role of product labelling in building user confidence in biosimilars in Europe
Published in: Volume 3 / Year 2014 / Issue 4
Author(s): European Biopharmaceutical Enterprises
Page: 188-92
Author(s): European Biopharmaceutical Enterprises
Page: 188-92
Abstract: The European Medicines Agency (EMA) has led the development of biosimilar regulatory pathways globally, tailoring their approach to meet the specific and scientifically determined needs of biosimilar development. However,… Read More »