November 21, 2016 11:45 am
The expectation of cyber security has to be met with the same fervor and drive that you strive to meet all your other clients’ expectations.
November 16, 2016 1:27 pm
New documents offer assistance to those in the medical device community.
November 16, 2016 1:36 pm
There are myriad challenges when bringing together the drug development and device development process.
November 16, 2016 1:39 pm
Fundamental training for contamination control.
November 16, 2016 2:17 pm
As we look into the future of the cleanroom industry, which is expected to change at its fastest rate ever, we examine how best practice can be better sustained to meet innovative heights.
November 16, 2016 1:06 pm
Develop the right sampling plan for your facility.
November 15, 2016 1:29 pm
Maintaining the quality of Purified Water and Water for Injection.
November 14, 2016 10:58 am
Cleanrooms play a crucial role in patient safety. Regulators around the globe are moving drug manufacturers toward continuous improvement with zero defects in mind. With injectable drugs, this specifically can mean limiting particulate levels — and the manufacturers of drug delivery systems must do their part to meet this challenge.
November 14, 2016 11:08 am
In traditional environmental monitoring workflows, single-bagged plates are de-contaminated and stored in the isolator. Space can be limited in the isolator, allowing storage of only a small supply of contact or settle plates. When this supply runs out, workflows are interrupted as new plates are prepared for use.
November 10, 2016 5:16 pm
Cleanroom glove and apparel manufacturers have many factors to consider. However, generally speaking, the needs of users come back to one common theme: the desire to minimize and control contamination, which comes in a variety of forms from biological to particulate matter or even nonvolatile and ionic residues on the surface of the glove.
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