Topics - Process Validation
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By Julie Larsen, BioTeknica, Inc.
Published November 9, 2012
10 Key Questions to Assess Inspection Readiness Read More »
By Klaus Ullherr, Robert Bosch GmbH
Published September 6, 2012
How will manufacturers and suppliers approach PFS? Read More »
By Aloke Das, Beroe Inc.
Published September 6, 2012
Implications on downstream biologics processing Read More »
By Gil Roth
Published August 29, 2012
$17 mil. deal adds to endotoxin, microbial portfolio Read More »
By Gil Roth
Published June 21, 2012
Will assess Daikyo Crystal Zenith technologies for containment Read More »
By Gil Roth
Published June 20, 2012
New program incorporates bio-services from preclinical to commercial Read More »
By Kuljit S. Bhatia, DPT Laboratories
Published May 30, 2012
A new business model for a volatile industry Read More »
By Martin Lush, NSF-DBA
Published May 4, 2012
Causes and prevention: What can we learn from the mistakes of others? Read More »
By William Downey, HighTech Business Decisions
Published May 4, 2012
Recent initiatives in biopharma contract manufacturing Read More »
By Andrea Wagner
Published April 4, 2012
Pairing the product, package and process for parenterals Read More »
By Ross Acucena and Randy Wilkins
Published April 4, 2012
Best practices for sterile filtration validation of re-use and extended-use processes Read More »
Published April 4, 2012
More opportunities, but greater regulatory scrutiny Read More »
By Paolo Mazzoni, PTM Consulting
Published March 7, 2012
Why we need a “robust” process mapping system Read More »
By Kristin Brooks, Associate Editor
Published March 7, 2012
Industry perspective from suppliers and manufacturers Read More »
