How to Achieve a Compliant and Effective Cleanroom Design and Facility Validation
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Category FDA Compliance;
Deadline: March 27, 2015 | Date: March 27, 2015
Venue/Country: Palo Alto, U.S.A
Updated: 2015-03-25 19:48:16 (GMT+9)
Call For Papers - CFP
This training program will discuss designing an effective cleanroom facility validation protocol and report, when and how to transition into the routine environmental monitoring processes, how to maintain a state of control within the cleanroom, and the routine environmental monitoring and excursion investigation processes.Why Should You Attend:This 90-minute training will provide participants an understanding of:The regulations guiding cleanroom facilitiesWhat constitutes an effective designCleanroom classificationHow a cleanroom validation should be structuredWho Will Benefit:Quality ControlManufacturing/ProductionSenior ManagementRegulatory AffairsQuality AssuranceComplianceInstructor Profile:Charity Ogunsanya has over 23 years of extensive experience within the pharmaceutical, biotechnology, biologics, cell-therapy, diagnostics, research and development, radio-pharmaceutical, contract manufacturing organizations (CMOs) and medical device companies.Note:Use coupon code 232082 and get 10% off on registration.For Registration:http://www.complianceonline.com/ensuring-a-compliant-and-effective-cleanroom-design-and-facility-validation-webinar-training-703875-prdw?channel=ourglocal
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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