Quality by Design and Extractable and Leachable Testing
February 26, 2015 - BioPharm Intl.
The author discusses the various ways in which a quality-by-design program can enhance the extractable and leachable assessment of a drug product.
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The Bullish Outlook for Biosimilars
February 26, 2015 - BioPharm Intl.
Feb 01, 2015
By Jill E. Sackman, PhD, Michael J. Kuchenreuther, PhD
BioPharm International
There are several impo
Labeling of Biosimilars
February 26, 2015 - BioPharm Intl.
EMA is under pressure to exert even tighter standards on biosimilars being marketed in Europe.
Feb 01, 2015
By Sean Milmo
Fermentation for the Future
January 30, 2015 - BioPharm International
Improving efficiency, value chain, quality, and protein complexity with advanced bioprocess development.
Jan 01, 2015
Ligand-Binding Assays and the Determination of Biosimilarity
January 29, 2015 - BioPharm Intl.
Implementation of Raw Material Control Strategies in the Manufact
January 29, 2015 - BioPharm International
The authors review efforts to limit polymer degradation without significantly impeding cell growth.
Jan 01, 2015
Technologies and Practices Must Evolve to Meet Demand
January 29, 2015 - BioPharm International
Jan 01, 2015 By Rita Peters
What Drove Biopharma Development in 2014?
January 16, 2015 - BioPharm Intl.
Process Development Forum
Improving PAT for Biologics
December 18, 2014 - BioPharm Intl.
The complexity of biopharma processes requires innovative solutions.
Dec 01, 2014
By Cynthia Challener, PhD
BioPh
Securing the Single-Use Supply Chain
December 18, 2014 - Pharmaceutical Technology
Dual sourcing is one of many possible solutions to securing the supply chain.
