The United States Pharmacopeia’s (USP) newer compliance guidelines for compounding pharmacies include more stringent requirements for cleanroom environmental monitoring. To better support customers’ ...
In the pharmaceutical industry, cleanrooms are categorized based on the level of airborne particle concentration necessary to meet the cleanliness standards required for the specific manufacturing ...
The shift toward personalized medicines poses new challenges in cleanroom protocols. Maintaining a sterile cleanroom environment and stringent cleanroom protocols in biopharmaceutical manufacturing ...
General conformance of environmental-monitoring data to Benford’s law must be proven before the principle can be used to ...
Biopharmaceutical environmental monitoring is a labor-intensive, time-consuming effort required by major regulatory agencies all over the globe. Pharmaceutical companies growing their production ...
Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points per month, manual data transcription and all too frequently ...
Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points per month, manual data transcription and all too frequently ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback