Switching from Reference to Biosimilar Products: An Overview of the European Approach and Real-World Experience So Far
Switching patients from a reference to a biosimilar product has become a primary topic of interest, with different approaches being undertaken by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). In European countries, substitution of a reference medicine with a bi...
Main Authors: | Anna La Noce, Marcin Ernst |
---|---|
Format: | Article |
Language: | English |
Published: |
European Medical Journal
2018-09-01
|
Series: | European Medical Journal |
Subjects: | |
Online Access: | https://www.emjreviews.com/rheumatology/article/switching-from-reference-to-biosimilar-products-an-overview-of-the-european-approach-and-real-world-experience-so-far/ |
Similar Items
-
Real-World Evidence on Etanercept Biosimilar SB4 in Etanercept-Naïve or Switching Patients: A Systematic Review
by: Hans C. Ebbers, et al.
Published: (2019-08-01) -
On the Regulatory Approval Pathway of Biosimilar Products
by: Jun Wang, et al.
Published: (2012-03-01) -
Authorisation of Non-Innovator Biotherapeutic (Biosimilar) Products in the USA
by: A. A. Soldatov, et al.
Published: (2019-03-01) -
SAFETY AND CLINICAL EFFICACY IN BIOSIMILAR SUBSTITUTION
by: João Pedro Fernandes, et al.
Published: (2015-01-01) -
Pricing and Reimbursement of Biosimilars in Central and Eastern European Countries
by: Paweł Kawalec, et al.
Published: (2017-06-01)