We often overlook compressed air as a potential source of clean room and product contamination. For pharmaceutical use, compressed air is considered to be a critical utility, as most of its applications involve a direct contact with the pharmaceutical product.
Join this webinar, where expert speaker Roger Cowan will help you understand the different types of contamination implicit in compressed air, and will discuss the ways to prevent your system from being affected by each type. He’ll outline the typical pharmaceutical compressed air system and its individual components, including engineering schematics.
Lastly, he’ll present a compilation of FDA/EU GMP Guidance, USP/EP and ISO air standards and cover sampling and testing methodologies for each of these specifications
Who Should Attend
Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.
Roger Cowan is the founder and owner of R Cowan Consulting Services LLC, a consulting company specializing primarily in the area of pharmaceutical contract manufacturing. He has 37 years’ experience in pharmaceutical quality assurance and manufacturing. In his career, Roger has held various manager / director positions in Quality Assurance, QC Laboratory, Technical Services Validation, Manufacturing, and Clinical Supply manufacturing and distribution. Roger has taught courses in microbiology...
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