Aseptic Processing Overview and Validation 2019
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Website https://www.compliance4all.com/control/w_product/~product_id=502328LIVE?channel=ourglocal_Feb_2019_S |
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Category Quality Assurance, Regulatory Affairs, manufacturing, environmental monitoring
Deadline: February 27, 2019 | Date: February 28, 2019
Venue/Country: Online, U.S.A
Updated: 2018-12-07 15:03:39 (GMT+9)
Call For Papers - CFP
Overview:This course will provide an overview of the requirements for aseptic and bulk manufacturing operations, including facility design, contamination controls and acceptable personnel behaviors.Why should you Attend:Explain the difference between Aseptic and Bulk processingUnderstand facility and personnel requirements necessary to maintain microbial controlExplain basic principles of microbiology and microorganism recovery in relation to cleanroom environmental monitoring (EM) and impact to productUnderstand the gowning requirements associated with different cleanroom classificationsAreas Covered in the Session:Review Clean Area BehaviorsPersonnel gowning requirementsGood clean area behaviors/practicesPractices to avoid – and whyWho Will Benefit:Engineering & ValidationFacilities / MaintenanceQuality AssuranceRegulatory AffairsSpeaker Profile:Kelly Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.Event Fee: One Dial-in One Attendee Price: US $150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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