Newsletter | November 14, 2019

11.14.19 -- Incentivizing U.S. Biosimilar Use In Oncology

 
Featured Editorial
What Incentivized These Oncology Clinics To Embrace Biosimilars?
 
By Anna Rose Welch, editor, Biosimilar Development

I reached out to Dr. Jeffrey Patton, the CEO of Tennessee Oncology and president of physician services and board member at OneOncology, to better understand the overall decision to implement Amgen's Kanjinti and Mvasi biosimilars, as well as which mechanisms he believes will help improve biosimilar usage in oncology in the months and years ahead.

Trends To Watch In China’s Biopharma Industry
 
By Vicky Xia and Leo Cai Yang, BioPlan Associates, Inc.

Fueled by the country’s large population and rapid urbanization, China’s biopharma segment has experienced double-digit growth for the past decade, and the landscape is poised for robust growth for the near future.

The Need For Enhanced Control Strategies In Biopharma Production
 
By Emil W. Ciurczak, Doramaxx Consulting

Biologics are the next great step for the pharmaceutical industries. The double-edged sword is that, as the molecules become more and more complex, our need for control and understanding becomes greater. 

Industry Insights
Scaling A mAb Production Process To A Single-Use Platform
White Paper | GE Healthcare Life Sciences

The transfer of a monoclonal antibody (mAb) production process between scales, often referred to as scale-up or scale-down, is a difficult task. This study reviews moving a monoclonal antibody production process from a microscale bioreactor to the Xcellerex XDR single-use platform.

Sponsor
 

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Solutions
Get The Best Monomer Recovery During Protein Purification
Bio-Rad Laboratories, Inc.
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