Biosimilars in Oncology: Insights Into the Development and Evaluation Process

In this slideset, Rowena Schwartz, PharmD, BCOP, discusses the regulatory standards and benchmarks necessary for the approval of therapeutic biosimilars.
Format: Microsoft PowerPoint (.ppt)
File Size: 397 KB
Released: June 9, 2017

Acknowledgements

Supported by independent medical education grants from
Pfizer Inc.
Sandoz Inc., a Novartis Division

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