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Article Welcome to the new Process Development Forum
August 15, 2013 Welcome to the new Bioprocess Development Forum (PDF) website. We launched www.ProcessDevelopmentForum.com two years ago as a new channel for information relevant to research…

Article QbD and PAT in Upstream and Downstream Processing
…l pharma companies in order to ensure a fast-track initiative from R&D to license to operate and market). The risk assessment includes a review and assessment of the products CQAs when manufactured o…

Article Addressing the Challenges in Downstream Processing Today and Tomorrow
Newer classes of biotherapies will require innovations in processing technology. By Glen R. Bolton, Bernard N. Violand, Richard S. Wright, Shujun Sun, Khurram M. Sunasara, Kathleen Watson, Johna…

Resource FDA’s Adverse Event Reporting System (AERS)
The FDA uses AERS to monitor for new adverse events and medication errors that might occur with these marketed products.

About
About Us Process Development Forum is an online resource for biopharmaceutical researchers, scientists, and process engineers what are interested in information on innovations and te…

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