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08.25.2010 -- Continuous Manufacturing for Secondary Processes: Leapfrog Time?

August 25, 2010

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Featured Articles

Continuous Manufacturing for Secondary Processes: Leapfrog Time?
By Rebecca Vangenechten and Ivo Backx, Siemens
Pharmaceutical secondary manufacturing has long stood in stark contrast to the drug discovery end of the business, as well as to other sectors, when it comes to innovation — such as continuous manufacturing. Is that about to change? Rebecca Vangenechten and Ivo Backx, from Siemens, argue that the coming decade could see secondary manufacturing not just catch up, but leapfrog other sectors, but that mindset will be a crucial factor.


Only Time Will Tell With Biotech QbD
By James Netterwald, Ph.D., Life Science Leader magazine
When manufacturing a pharmaceutical product, there are various attributes that contribute to overall quality, including solubility, toxicity, and uniformity. These attributes are affected by process parameters, such as temperature inside of a bioreactor or gas chamber, internal pressure of a bioreactor, concentration of catalysts or raw materials, and diffusion rates.

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Brochure: Closure Processing Systems (CPS)
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Industry News

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PAREXEL Introduces Temperature Recording Solution For Study Drug Transportation
Cumberland Pharmaceuticals Announces Extension Of FDA Review Of Supplemental New Drug Application
Governor O'Malley Announces State Grants Available For Maryland Bio Companies
Ready-To-Use Gene Delivery Tools
Life Technologies And SG Biofuels Complete Sequence Of Jatropha Genome
3SBio And Isotechnika To Develop And Commercialize Voclosporin In China
Pharmasset Initiates Phase 2b Clinical Trial Of PSI-7977 For Chronic Hep C
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Bulletin Board

Industry Events

Webinar: Media And Buffer Prep Powder Handling For The Biopharmaceutical Industry
Presented By ILC Dover
September 1 | 11:00 EDT

IBC's BioProcess International™ Conference And Exhibition
September 20 to 24 | Rhode Island Convention Center, Providence RI

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