Continuous Microbial Monitoring
“Annex 1 provides general guidance that should be used in the design and control of facilities, equipment, systems and procedures used for the manufacture of all sterile products applying the principles of Quality Risk Management (QRM), to ensure that microbial, particulate and endotoxin/pyrogen contamination is prevented in the final product”. Continuous viable air monitoring in […]
Aseptic Pharmaceutical Manufacturing
Aseptic Compounding Tools Portable Airborne Particle Counters Temp. Relative Humidity Sensors Differential Pressure Sensors Portable Viable Sampling Remote Particle Counting Remote Viable Sampling Aseptic Manufacturing Operations Aseptic pharmaceutical manufacturing Is a highly regulated process that involves the production of sterile drugs under controlled conditions to ensure the safety and efficacy of the drugs. The manufacturing […]
