Implications of the FDA draft guidance on biosimilars for clinicians: what we know and don't know

J Natl Compr Canc Netw. 2013 Apr 1;11(4):368-72. doi: 10.6004/jnccn.2013.0052.
No abstract available

MeSH terms

  • Biosimilar Pharmaceuticals / pharmacokinetics
  • Biosimilar Pharmaceuticals / therapeutic use*
  • Drug Approval / methods
  • Drug Substitution
  • Health Knowledge, Attitudes, Practice*
  • Health Plan Implementation / legislation & jurisprudence
  • Health Plan Implementation / methods
  • Humans
  • Off-Label Use / legislation & jurisprudence
  • Physicians / legislation & jurisprudence
  • Practice Guidelines as Topic*
  • Research Report
  • Therapeutic Equivalency
  • United States
  • United States Food and Drug Administration / legislation & jurisprudence*

Substances

  • Biosimilar Pharmaceuticals