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13 Products
12 Products
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Join our experts at the upcoming virtual Cleaning Validation Summit hosted by PharmaEd Resources Inc.
Personnel are typically the primary source of contamination in cleanrooms. This is true at pharmaceutical,
The PDA Australia Chapter are delighted to invite you to join our first event for
Biofilm formation in process equipment presents challenges and may lead to serious consequences in GMP
An effective cleaning and disinfection program is critical to controlling the bioburden in a cleanroom.
The FDA conducted approximately 17,671 inspections in Fiscal Year 2018, amounting to roughly 1400 inspections/month
This workshop will provide an overview of microbiology principles in steam sterilization and application, as well as autoclave Performance Qualification, regulatory
This presentation will focus on the current regulations, guidelines, method and standards available for disinfectant
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