BEGIN:VCALENDAR VERSION:2.0 PRODID:icalendar-ruby CALSCALE:GREGORIAN BEGIN:VEVENT DTSTAMP:20240329T064204Z UID:3bcd66ee-89d1-4ae2-858e-fd18fd5070ae DTSTART:20210301T130000 DTEND:20210302T130000 CLASS:PRIVATE DESCRIPTION:
Overview
\n\nThis webinar will take y ou through the primary sources of compressed air contamination. It will al so detail GMP standards and requirements pertaining to compressed air qual ity.
\n\nThe design\, construction and monitoring of a compressed ai r system is essential for maintaining a quality system without product con tamination. Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharm aceutical product. Proper testing of compressed air quality according to i nternational standards is important for both validation and ongoing monito ring of the system as well.
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\n\nWhy Should You Attend
\n\nCompressed air is often overlooked as a potential source of clean room and product contamin ation. This webinar will give you an understanding of the different types of contamination inherent in compressed air and how to prevent each from a ffecting your particular system.
\n\nA detailed description of a typ ical pharmaceutical compressed air system with its individual components w ill be provided. Engineering schematics will also be included. All compone nt functions will be detailed with recommendations as to which component t ype is considered optimal.
\n\nThe four contamination sources in com pressed air will be discussed. They are:
\n\nSolid par ticulate
\nWater content
\nTot al oil content
\nMicrobial bioburden
\nFor each of these\, the presentation will discuss cause and effe ct. Suggestions will also be provided for preventing contamination. Finall y\, a compilation of all FDA/EU GMP guidelines\, USP/EP and ISO air standa rds will be presented. Sampling and testing methodology for each of these specifications will be discussed as well.
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\n\ nSession Highlights
\n\nCompressed Air - Importance of Quality
\nPharmaceutical Compre ssed Air System Design
\nContamination Types and Sou rces
\nContamination Prevention
\nInternational GMP Testing Standards
\nTesting Me thods and Specifications
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\nWho Will Benefit
\n\nThis webinar will provide valuable assistance to all personnel in pharmaceutical manufacturing and c ompounding pharmacies:
\n\nQuality assurance
\n \nEnvironmental monitoring
\nMicrobiolo gy
\nManufacturing
\nValidatio n
\nEngineering
\nMaintenance< /p>\n