Assess Your Laboratory - Based on the FDA System Based Inspections
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Deadline: June 26, 2018 | Date: June 26, 2018
Venue/Country: Online, U.S.A
Updated: 2018-06-13 18:04:49 (GMT+9)
Call For Papers - CFP
The Quality Control Laboratory plays an important part role in the production and release of a drug product regulated by the FDA. Inspectional observations of non-compliant laboratory operations are high on the list of most frequent regulatory observations. As the industry focuses more on the quality system and product and test method lifecycle, the operation of the laboratory unit becomes more visible. The laboratory should have active programs in which the laboratory is routinely assessed for compliance to applicable regulations and standards.Venue:OnlineSpeaker Name: Jerry LanesePrice : $ 239Wednesday, June 26, 2018 EST 13:00Duration : 90 MinutesTel: +1-844-216-5230Email: support
compliancetrainingpanel.comKeywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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