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BioPharm International

BioPharm International-12-01-2009
Volume22
Issue 12

BioPharm International, December 2009 (PDF)

QbD in Practice–Part 2: The Regulatory Filing

To view a PDF of this article from the BioPharm International archives, click this link

Articles in this issue
BioPharm International, December 2009 (PDF)
Jim_Miller-646886-1408635855836.jpg
CDMOs Benefit from the Growing Biologics Market
DisAD_Fig1-646885-1408635858745.jpg
Disposables in Rapid Response Manufacturing: The Next Steps
Fig1_norm_operating_range-646892-1408635835700.jpg
Quality by Design for Biotechnology Products—Part 2
Eric_Langer-646887-1408635853279.jpg
Licensing of Expression Systems
Jill_Wechsler-646890-1408635841276.jpg
The Promise and Perils of Vaccines

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