Clean Aira —-Iso ——> 0.5 um Particles —Microbiological ——Microbiological*
Clasification—Designation—Per Cubic——Ative Air Action leve– Stteling plate *
100—— —-5———-3520————1—————–1
1000—– —-6———35200———–7—————–3
10000— —–7———352000———10—————-5
100000—- –8———-3520000——-100————–50
Action Lvel CFU per 4 HRS*
Also see Pharmaceutical process validation
This Website is a Guide for Pharmaceutical Manufacturing pharmacy students pharmacy colleges and pharmacists pharmaceutical companies in health care.
This Website is a Guide for Pharmaceutical Manufacturing pharmacy students pharmacy colleges and pharmacists pharmaceutical companies in health care.
Guidelines for Standard operating procedure SOP for microbiology and aseptic techniques for manufacturing of sterile pharmaceuticals , cgmp guidelines for pharmaceuticals, pharmaceutical validations
Regulatory affairs in pharmaceutical industry
Following are some of articles which will be useful for you in further understanding of aspects of sterile dosage form manufacturing
