FDA Regulations for Environmental Monitoring (EM) Program
Website https://www.complianceonline.com/environmental-monitoring-em-program-basics-webinar-training-704377- |
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Deadline: March 04, 2019 | Date: March 04, 2019
Venue/Country: U.S.A
Updated: 2019-01-25 15:55:22 (GMT+9)
Call For Papers - CFP
This 90-minute webinar will discuss various broad and critical aspects of an effective EM program such as the phases of a cleanroom EM program–pre-monitoring of a cleanroom prior to facility validation, implementation of routine EM using facility validation data and post-validation. Procedural steps, content of a robust EM program such as handling, incubation, documentation, management and trending of data, EM excursion investigation and product impact and disposition will be discussedKeywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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