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Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results

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This training on pharmaceutical laboratory OOS investigations will explain how to recognize and address atypical or out of specification results, using approaches which have been recommended by regulatory authorities, performing appropriate investigations.

Speaker
Instructor: Gregory Martin
Product ID: 702360

Why Should You Attend:

Upon completion of this course the attendee should:

  1. Be familiar with various terms associated with investigations of atypical or out of specification results, and how to document those investigations.
  2. Be familiar with the FDA Guidance for Industry on Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production and how to apply it in laboratory situations.
  3. Be able to create a Laboratory Investigation Checklist and effectively document an investigation, including rationale and results.
  4. Know the importance of Corrective and Preventative Action (CAPA) and be able to identify appropriate CAPAs.
  5. Understand practical strategies to utilize outcomes from investigations for continuous improvement and reduction of future OOS results.

Areas Covered in the Seminar:

Who Will Benefit:

The following personnel in pharmaceutical laboratories will benefit from this training:

Instructor Profile:

Gregory Martin, is President of Complectors Consulting which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. He has particular interest in QbD/Lean approaches to dissolution testing, impurity methods, method lifecycle (development/validation/transfer) and instrument qualification, and is passionate about using good science and sound logic to achieve high quality results, consistent with cGMPs, while minimizing resources. Mr. Martin has over 25 years experience in the pharmaceutical industry and was Director of Pharmaceutical Analytical Chemistry (R&D) for a major PhRMA company for a number of years.  In addition, he has volunteered for the USP for over 10 years, and currently serves as Vice Chair of the General Chapters – Physical Analysis Expert Committee, and serves on Expert Panels on Validation and Verification, Weights and Balances and Use of Enzymes for Dissolution Testing of Gelatin Capsules.  He is also Chair-elect of the AAPS In Vitro Release and Dissolution Testing Focus Group. He serves on the Editorial Advisory Board of the Journal of Validation Technology and Journal of GXP Compliance.

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Training Options Training Duration = 120 Min
$599.00 Get Training CD Only
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days