Single-use systems offer essential advantages – especially when standardized single-use sets are employed. They can be implemented quickly and affordably while reducing complexity.
Can performing tests and sharing outcomes help to build a common approach and standard that will begin to standardize this important containment protective measure?
A failed chamber mapping study can lead to unnecessary costs in valuable biopharmaceutical production time or regulatory and product quality issues.
There exists two key methods for controlling serious outbreaks of transmissible diseases: therapeutic countermeasures and transmission control through isolation and containment.
The move from sterility testing within LAF safety cabinets to those in aseptic isolators has resulted in a marked decrease in false positives.
The use of aqueous cleaning in medical device manufacturing can provide numerous benefits in terms of efficacy, minimal surface contact and reduced residue potential, and easier cleaning validation.
The use of aqueous cleaning in pharmaceutical manufacturing can provide numerous benefits in terms of effectiveness, minimal surface residue, and easier cleaning validation.
Systems should be analyzed not only for their basic ability to contain the powders of interest, but also for how efficiently they integrate into the production process. For instance, will the system help to eliminate productivity bottlenecks, decrease material waste and the cost of raw materials, and simplify the changeover of the line to new products?
“Closed system filling” is a new set of processing controls for a sterile filling process that eliminates potential microbiological contamination from environmental and operator sources.
Biosafety cabinets are a vital part of research, hospital, and industry laboratories worldwide, creating a clean and ventilated workspace for research, development, diagnosis, and drug preparation.
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