Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing
Website https://www.complianceonline.com/equipment-qualification-dq-iq-oq-pq-process-validation-vmp-seminar- |
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Deadline: August 08, 2020 | Date: August 18, 2020-August 19, 2020
Venue/Country: U.S.A
Updated: 2020-07-03 03:37:52 (GMT+9)
Call For Papers - CFP
The various regulatory agencies have expectations that pharmaceutical manufacturers will demonstrate control over their manufacturing equipment. The FDA's findings of deficiencies concerning equipment validation indicate the agencies expect definitive evidence that the equipment qualification and validation schedules of a facility will satisfactorily control their manufacturing processes. Examples of FDA form 483 findings for equipment qualification and validation indicate deficiencies in many of these studies.The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for equipment qualification and validation in your manufacturing facility?Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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