Fill/Finish

Mar 13, 2013
Pharmaceutical Technology
The growth in biologics drugs and vaccines is leading to greater demand for prefilled syringes, which provide greater safety and convenience for healthcare workers and patients.
Jan 01, 2013
Pharmaceutical Technology Europe
By Pharmaceutical Technology Editors
PharmTech speaks to Ray O'Connor from the National Institute for Bioprocessing Research and Training (NIBRT) for an overview of aseptic processing.
Jul 05, 2012
ePT--the Electronic Newsletter of Pharmaceutical Technology
By Pharmaceutical Technology Editors
GSK Extends Deadline for Tender Offer to Acquire Human Genome Services; Sartorius Opens New Filter, Aseptic-Bag Production Facility in Puerto Rico; and More.
Jun 02, 2012
Pharmaceutical Technology
By Pharmaceutical Technology Editors
How to avoid invisible and airborne contamination.
May 01, 2012
Pharmaceutical Technology
By Pharmaceutical Technology Editors
Closed-vial technology is an alternative to traditional glass vial filling that reduces the risk of contamination for the patient, simplifies the filling process, and provides easier handling for healthcare providers.
Apr 11, 2012
ePT--the Electronic Newsletter of Pharmaceutical Technology
By Pharmaceutical Technology Editors
FDA has released a final guidance describing cGMP for preparing media fills for validation of aseptic preparations for positron emission tomography drugs.
Dec 01, 2011
Pharmaceutical Technology Europe
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.
Oct 19, 2011
Equipment and Processing Report
By Pharmaceutical Technology Editors
The future, and increasingly the present, for aseptic operations is isolated robotics. Companies that wish to gain competitive advantages in their operations are stepping up and taking notice.
May 01, 2011
Pharmaceutical Technology
The authors question certain aspects of the industry's current regulatory-compliance strategy and suggest that aseptic-process control and evaluation should be revised.
Apr 20, 2011
Equipment and Processing Report
By Pharmaceutical Technology Editors
We want to fill one of our oxygen-sensitive products inside an isolator system. Can we run an isolator with pure nitrogen and defined humidity?
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