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Assess Your Laboratory - Based on the FDA System Based Inspections

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Website www.compliancetrainingpanel.com | Edit Freely

Category

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:Online

Speaker Name: Jerry Lanese

Price : $ 239

Wednesday, June 26, 2018

EST 13:00

Duration : 90 Minutes

Tel: +1-844-216-5230

Email: support@compliancetrainingpanel.com


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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