Articles
Tools to Keep Pharma Fluids Flowing
An assortment of pump and valve innovations help provide clean process efficiencies.
Post Date: 01/15/2013
Author: Katie Weiler, Managing Editor
Trouble Shooting Depth Filtration
Some common scenarios (and their root causes)
Post Date: 10/03/2012
Author: Brittany Nixon, 3M Purification
Are Single-Use Standards Stuck? And Is That a Bad Thing?
Efforts to enact meaningful standards for single-use bioprocessing technologies move at a snail's pace, with no clear path forward, experts say.
Post Date: 06/21/2012
Author: Paul Thomas, Senior Editor
Biopharma's Flexible Imperative
Business forces, bioterror and pandemic risks demand new approaches to manufacturing.
Post Date: 06/06/2012
Author: Robert F. Dream, Principal, HDR Company, LLC
Bioprocess Filter 411: A Look at New Products for 2012
Solution providers churn out new and improved products in the heated market for upstream and downstream filtration technology.
Post Date: 05/08/2012
Author:
With a Full Range of Products, EMD Millipore Turns Its Attention to Solutions
The company aims to leverage the expertise it has always had in-house, yet hadn’t fully capitalized on with the pharma industry, says VP Christophe Couturier.
Post Date: 05/02/2012
Author: Paul Thomas, Senior Editor
The Pulse of Pharmaceutical Manufacturing
The big picture has changed very little in ten years. While pointing out root causes, observers also see reasons for optimism.
Post Date: 04/04/2012
Author: Agnes Shanley, Editor in Chief
Imaging the Blending Process
Hyperspectral imaging can be used to optimize blending, by monitoring the distribution of excipients and APIs in formulation.
Post Date: 01/03/2012
Author: Gabor Kemeny and Gina Stuessy, Middleton Research
Process Validation Guidance: A Bad Fit for Aseptic Processing?
“Science-based” is well and good, but FDA’s guidance may create confusion.
Post Date: 09/28/2011
Author: Paul Thomas, Senior Editor
Risk Management in Pharmaceutical Microbiology
At look at how HACCP and FMEA can make a difference in the pharma micro lab.
Post Date: 09/21/2011
Author: Tim Sandle, Head of Microbiology, Bio Products Laboratory
Therapeutic Dose: Facilius per Partes in Cognitionem Totius Adducimur
We are more easily led part by part to an understanding of the whole. –Seneca
Post Date: 07/20/2011
Author: Emil W. Ciurczak, Contributing Editor
Maintaining Integrity: Effects of SIP Sterilization on PTFE Valve Diaphragms
As PTFE diaphragms are subjected to more aggressive sterilization and cooling conditions, they are more prone to failure from cracking, splitting, deformation and SIP steam-induced blisters.
Post Date: 06/01/2011
Author: Steve Pitolaj, Principal Engineer, and Jim Drago, P.E., Garlock Sealing ...
Bioprocess Filtration: Debating Post-sterilization Integrity Testing
At PDA 2011, at issue was whether current EMA guidelines are rational or risky; also, a look at new filtration products on the market.
Post Date: 05/18/2011
Author: Paul Thomas, Senior Editor
pH: Are You in Control of a Moving Target?
pH is a deceptively simple measurement; its control can be extremely challenging in both upstream and downstream biopharmaceutical manufacturing.
Post Date: 04/05/2011
Author: Jim Wilkins, Sensorin, Inc.
Controlled Ice Nucleation Moves into Manufacturing
Two viable techniques exist for better lyo control in commercial processes, says UConn’s freeze-drying guru.
Post Date: 02/15/2011
Author: Paul Thomas, Senior Editor
Microbial ID Habits, Under the Microscope
A look at what microbiologists do and want, by the numbers, and commentary from consultant Pascal Yvon.
Post Date: 09/10/2010
Author: Paul Thomas, Senior Editor
Continuous Low Moisture Wet Mass Granulation: A Demonstration of Potential
In text, illustrations, and video, Bren Kindelsperger makes the case for continuous wet mass granulation as an alternative to traditional methods of tablet and pill formulation.
Post Date: 07/21/2010
Author: Dr. Bren W. Kindelsperger, Readco Kurimoto LLC
PDA 2010: A Glimpse into the Single-Use Future
Maik Jornitz envisions the vast potential of single-use biotechnologies.
Post Date: 04/06/2010
Author: Paul Thomas, Senior Editor
Taking the Plunge to Harmonize Pharmaceutical Regulations
Within the past five years, more of world's regulatory agencies and pharmacopeias have gotten on the same wavelength.
Post Date: 03/04/2010
Author: Agnes Shanley, Editor in Chief
A Business Case for Isolation Technology
Every sterile facility is unique, but a recent Jacobs study suggests that advanced isolation technology pays dividends in the long run.
Post Date: 01/11/2010
Author:
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