Submitted: 5 December 2017; Revised: 7 December 2017; Accepted: 8 December 2017; Published online first: 21 December 2017
There are some major differences between USA and Europe regarding how they view interchangeability of biologicals/ biosimilars. In fact, there is a lack of harmonization around the world when it comes to how different countries or regions approach interchangeability of biosimilars .
In the US, the Biologics Price Competition and Innovation Act of 2009 (BPCI Act) creates an abbreviated licensure pathway for biological products shown to be biosimilar to or interchangeable with a Food and Drug Administration (FDA) licensed reference product. Interchangeability is defined in law as part of the BPCI Act as:
‘the biological product may be substituted for the reference product without the intervention of the healthcare provider who prescribed the reference product’.
FDA defines interchangeability as:
FDA may approve a biological product as interchangeable, see Table 1. Although individual states control the act of pharmacy-level substitution. The agency issued draft guidance on interchangeability in January 2017  and more recently extended the comment period on the guidance .
As of 1 July 2017, 35 states and Puerto Rico have passed laws allowing substitution by a pharmacist if the biosimilar is considered interchangeable and is covered under an insurer’s pharmacy benefit . However, despite issuing draft guidance on interchangeability in January 2017 , to date FDA has yet to approve a biosimilar as interchangeable with its reference biological.
The European Commission (EC) has defined interchangeability in a consensus information document on biosimilars  as:
‘the medical practice of changing one medicine for another that is expected to achieve the same clinical effect in a given clinical setting and in any patient on the initiative, or with the agreement of the prescriber’.
Substitution is considered to be:
In the EU, decisions on the interchangeability or substitution of biosimilars and originator biologicals are not made by the European Medicines Agency (EMA), but at the national level, see Table 1. This is the case, despite the fact that biosimilars developed in line with EU requirements are considered by EMA to be therapeutic alternatives to their reference biologicals .
Automatic substitution of biosimilars is therefore not routinely practised in Europe, although in some Member States the use of biosimilars has been actively facilitated by national and local tender systems.
Competing interests: None.
Provenance and peer review: Article abstracted based on published scientific or research papers recommended by members of the Editorial Board; internally peer reviewed.
Michelle Derbyshire, PhD, GaBI Online Editor
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