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Postmarketing Safety of Biosimilars: Current Status, Challenges, and Opportunities in the Spontaneous Reporting

Abhishek Singh1, Muthusamy Kalaivani1, Sushma Srivastava2

  • 1Biologics Section, Indian Pharmacopoeia Commission, Ministry of Health and Family Welfare (Government of India), Ghaziabad, India.

Therapeutic Innovation & Regulatory Science
|September 28, 2019
PubMed

Keywords:
EUUSFDAadverse drug reactionsbiosimilarspharmacovigilancespontaneous reporting system

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