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How to Investigate Deviations
and Failures Effectively
Conducted by Gamal Amer, Ph.D.
Principal - Premier Compliance Services, Inc.
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Investigation of failures and deviations in the pharmaceutical industry is a regulatory requirement. Recording the deviations and investigating their cause is but one step to meet the regulatory requirements. Correcting the issue based on risk assessment and understanding of the science as well as ensuring that the corrective actions are implemented within the appropriate time frame is another step.
Follow-up of the actions to ensure they are completed effectively and the fact that no new issues have been introduced is what completes the activities. A summary report must be developed, reviewed, and approved by the quality unit. Process monitoring, Quarterly Review of all deviation reports as well as Annual Product Reviews (APR) are the tools necessary to ensure that negative trends do not develop and that the manufacturing process remains under control.
By participating in this seminar you will learn:
- What the applicable regulatory requirements are
- What constitutes a deviation/discrepancy/failure
- What are the various types of deviation you may encounter
- How to conduct an investigation
- How to use risk assessment as a tool to define the appropriate corrective and preventive actions
- How to prepare a deviation summary report
- Why product reviews are critical
This seminar was conducted using GotoMeeting.com and is presented by Gamal Amer, Ph.D., an industry expert on this and other compliance related topics.
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Gamal Amer, Ph.D.
Gamal Amer, Ph. D. is Principal at Premier Compliance Services, Inc.; Management Consultants for compliance and manufacturing operations performance in the life sciences industry. He holds a Ph. D. in Chemical Engineering and has over two decades experience in the Pharmaceutical and related industries. He has held positions of increased responsibility with leading pharmaceutical, consumer product and engineering consulting firms over the years. His experience includes comprehensive process design in bulk pharmaceutical manufacturing, biotechnology manufacturing, pharmaceutical solid dosage manufacturing and containment of potent and radioactive therapeutics. He is also experienced with facility development for therapeutic products operations.
Dr. Amer is a recognized expert in GMP compliance and validation. He has consulted for many of the leading pharmaceutical, biotechnology and medical device manufacturers. He has lectured extensively in the US, Europe, Asia and the Middle East, taught many courses, and authored many papers which were published in peer reviewed publication. He is a member of ISPE, PDA, ACS and AIChE.
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