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April 18, 2013
PIERRE FABRE MEDICAMENT PRODUCTION has 22 years experience in isolator technology for aseptic filling of high potent freeze-dried injectable products.
September 01, 2012
There is no harmonized guidance on pre-use integrity testing of sterilizing filters, prompting discussion among users as to whether such testing is necessary.
August 15, 2012
Recycling is becoming a viable option for disposal of single-use systems.
August 02, 2012
Budgets for biopharmaceutical activities are gaining in select functional areas except outsourcing.
April 02, 2012
Critical issues that should be considered when scaling up a hot-melt extrusion process.
March 02, 2012
The standardization of upstream and downstream bioprocessing is growing, but several kinks need to be ironed out.
February 02, 2012
Experts discuss solutions for filter bacterial retention and related challenges. Contains online bonus material.
February 01, 2012
This column will address some of the questions on how single use systems are sterilized by gamma irradiation and what documentation may be requested by regulators.
December 01, 2011
Jerold Martin, senior vice president global technical affairs, at Pall Life Sciences, explains the importance and impact of single-use systems in sterile environments.
Contamination is almost always related to human error and there is a clear drive to reduce human implications in aseptic operations. This can be achieved in multiple ways.