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Webinar On Method Validation: Utilizing Quality by Design

Methods discussed in this session include assessment of method design, repeatability and reproducibility, improving method robustness and measurement process control. Methods for assessing that amount of product variation that can be attributed to the manufacturing process, sampling procedures and test method are also presented.

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Webinar On Method Validation: Utilizing Quality by Design

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  1. ContactUs:416-915-4458 Webinar On Method Validation: Utilizing Quality by Design and Risk in Implementation Presented By Dr. Ronald D. Snee Scheduled On :  Wednesday, April 29, 2015 at 13:00 Hrs EDT Hosting By Compliance Trainings Please visit us at https://compliancetrainings.com

  2. ContactUs:416-915-4458 WeEmpower,YouComply! Method Validation: Utilizing Quality by Design (QbD) and Risk in Implementation Product Id FDB1431 Category Food, Drugs & Biologics Wednesday, April 29, 2015 at 13:00 Hrs Scheduled On Duration 60 Minutes Speaker Dr. Ronald D. Snee Login at https://compliancetrainings.com/siteengine/Login.aspx WebinarDescription: Pharmaceutical industry is experiencing a growing need to improve performance driven by global competition and the increasing impact of information technology. FDA’s Process Validation Guidance calls for continued process verification which applies to both manufacturing and measurement processes. How to go about this improvement in a systematic, focused and sustainable manner is the question. Fortunately a world-class body of improvement technology exists known as Quality by Design (QbD); a science and data-based approach that builds quality into products and processes during development, validation and operations. A characteristic of good science is good data. Quality data are arguably more important today than ever before. Using a series of case studies and examples it will be shown how QbD can be integrated into a holistic approach that can be used to effectively design and improve laboratory processes enabling prompt, successful method validation. Methods discussed in this session include assessment of method design, repeatability and reproducibility, improving method robustness and measurement process control.

  3. Methods for assessing that amount of product variation that can be attributed to the manufacturing process, sampling procedures and test method are also presented. The concepts and methods involved will be introduced and illustrated with pharmaceutical and biotech case studies and examples. Areas Covered in the Session : • Participants in the webinar will learn how to improve test method performance by: • Rapid design and development of test methods using statistical design of experiments  • Improving measurement quality using Gage Repeatability and Reproducibility studies • Developing measurement systems that are robust to variations in method use • Controlling measurement variation by using control samples and statistical process control techniques • Identifying how much of the total variation is due to the manufacturing process, the sampling procedure and the test method Who Will Benefit : • Executives and Managers engaged in Pharmaceutical and Biotech Research and Development • Quality Assurance Personnel • Regulatory Affairs Professionals • Test Method Development and Validation Personnel • Quality Engineers • Process and Manufacturing Engineers • Research and Development Scientists • Operations Excellence Professionals • Biologists and Microbiologists • Chemists and Chemical Engineers • Anyone with a desire to learn the fundamentals of methodical performance improvement

  4. Speaker Profile Ronald D. Snee, PhD, is Founder and President of Snee Associates, a firm dedicated to the successful implementation of process and organizational improvement initiatives. He provides guidance to senior executives in their pursuit of improved business performance using Quality by Design, Lean Six Sigma and other improvement approaches that produce bottom line results. Prior to his consulting career he spent 24 years at the DuPont Company in a variety of assignments including pharmaceuticals. He has been developing and applying QbD methodologies for more than 30 years. His recent application and research on QbD has produced more than ten articles on use of QbD in Pharma and Biotech. He has also coauthored 2 books on the methods and tools of QbD and speaks regularly at conferences and meetings on the subject. He teaches QbD and related methodologies as an Adjunct Professor at Temple University School of Pharmacy and Rutgers University Pharmaceutical Engineering program. To Register This Webinar Please Visit https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1431 Contact Us For Immediate Assistance @ 416-915-4458 or Mail Us At uttam@compliancetrainings.com support@compliancetrainings.com

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