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Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes

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Website https://www.complianceonline.com/performing-a-effective-and-compliant-sterility-failure-investigatio | Edit Freely

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Deadline: February 20, 2019 | Date: February 20, 2019

Venue/Country: U.S.A

Updated: 2019-01-19 04:05:06 (GMT+9)

Call For Papers - CFP

This training program will highlight mistakes often made when corrective and preventative actions are not clearly identified and applied during a manufactured product sterility test failure investigation because an ineffective investigational procedure and tool was used to conduct a sterility test failure investigation. The webinar will also illustrate how avoiding such common mistakes will ensure that these types of products meet the sterility requirements USP and other regulatory guidelines applicable to finished products, bulk drug substance, raw materials or excipients.

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