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Acceptance Sampling - Methods and ApplicationsAcceptance Sampling - Methods and Applications by John Robinson





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Acceptance Sampling - Methods and ApplicationsAcceptance Sampling - Methods and Applications by
Article Posted: 02/25/2014
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Acceptance Sampling - Methods and ApplicationsAcceptance Sampling - Methods and Applications


 
Health
Summary:

GlobalCompliancePanel to hold RAPS-approved, two-day, in-person seminar in Boston, MA on the topic, “Acceptance Sampling – Methods and Applications” on March 6 and 7, 2014 (Thursday & Friday). Dan OLeary, President of Ombu Enterprises will be the speaker at this two-day session. This course has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Venue, date and timings:

The venue for this seminar is Courtyard Boston Logan Airport Hotel 225 William F. McClellan Highway – Boston, Massachusetts 02128. The seminar will be on March 6 and 7, 2014, from 9 A.M to 6 P.M EST.

What the seminar is about:

This unique hands-on course provides attendees with a solid understanding of acceptance sampling methods and their application to manufacturing. The course delivers tools, templates, and insight that will allow participants to choose and implement the best sampling methods for their application. Many companies use acceptance sampling as a standard business practice. The most common applications use attribute sampling based on ANSI/ASQ Z1.4 and Zero Acceptance Number Sampling Plans by Nicholas L. Squeglia. These common methods are not always the best approaches. This seminar will expose participants to a variety of methods and help them understand when to use them. Although primarily many of the examples come from medical device manufacturing because of the rigid regulatory structure; the methods apply in aviation, defense, and other manufacturing settings, as well. Many companies have procedures and programs that fall short of the regulatory requirements and good statistical practice. Because of this reason, they could invite a 483 or even a Warning Letter from the FDA. QMS audits may result in nonconformances that need to be addressed. In other cases, the firm may not use the best methods, resulting in waste of resources. This two-day hands-on course provides a clear understanding, with many exercises, of the methods and underlying statistics for acceptance sampling. As part of the practical implementation, the course explains common standards such as Z1.4 for attribute sampling and Z1.9 for variables sampling. In addition, the course covers other, less well-known methods such as sequential sampling, continuous sampling, and chain sampling.

About the Speaker:

Dan is the President of Ombu Enterprises, LLC. Started in late 2008, Ombu is a company that offers small manufacturing companies training and execution in operational excellence with a focus on analytical skills and a systems approach to operations management. Ombu handles issues relating to Operations and Quality. It offers education, training and execution in operational excellence. Dan has more than 30 years’ experience in Quality, Operations and Program Management in regulated industries including aviation, defense, medical devices, and clinical labs. He has a Master’s Degree in Mathematics from University of Maine; is an ASQ certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer, and Six Sigma Black Belt, and is certified by APICS in Resource Management. Prior to his association with Ombu, Dan has held many positions, including being Director, Program Office at Quest Diagnostics, Inc., Vice President of Operations at S&S Bioscience, Inc. and Business Process Executive – Manufacturing at Marconi Medical Systems.

The agenda:

The seminar will have the following agenda: Day 1 –Agenda Lecture 1: Introduction/Fundamentals - Regulatory Requirements Lecture 2: Introduction/Fundamentals - Statistics Lecture 3: Sampling Concepts Lecture 4: Attribute Sampling using Z1.4 Lecture 5: Attribute Sampling Using the Dodge-Romig System Day 2 –Agenda Lecture 6: Variables Sampling Using Z1.9 Lecture 7: Sequential sampling plans Lecture 8: Continuous sampling plans (CSP) Lecture 9: Skip-lot sampling plans (SkSP) Lecture 10: Chain sampling plans (ChSP) Lecture 11: Applications

For whom:

This seminar will benefit: a.Quality Managers b.Quality Engineers c.Supplier Quality Engineers d.Quality Analysts e.Production and Process Engineers f.Design and Development Engineers g.Verification and Validation

About GlobalCompliancePanel:

GlobalCompliancePanel (GCP) is a specialized offering from NetZealous LLC, a Technology and Business Process Solutions and Services Company registered in Fremont, CA. It is a fountainhead for Continuous Professional Education, compliance training and consulting. GCP offers a broad range of high quality regulatory and compliance-related services relating to Medical Devices, Pharmaceutical, FDA, Food, PCI industries, and SOX. Some of the Governing Areas its webinars cover are GxP (Manufacturing/Clinical/Lab), EU and ISO. These seminars are an extension of online trainings, at which GCP has conducted around 700 webinars since inception on a variety of topics for these industries /verticals. More than 30,000 professionals have benefited from these trainings. GlobalCompliancePanel’s trainings are focused, flexible and tailored to the client’s need. This is the next in a series of regulatory and compliance related seminars that GlobalCompliancePanel has been organizing all over the US. Its previous seminars have met with resounding success. GlobalCompliancePanel’s seminars have helped participants reach their career milestones. In bringing globally renowned experts in the field of regulatory compliance and executives in the industry together, GlobalCompliancePanel fosters a learning experience. With trainings that are focused and relevant, GlobalCompliancePanel seeks to serve as a bridge in the area of continuous professional education for regulatory and compliance-related fields.

Price:

Register now and save $200. (Early Bird) Until January 10, Early Bird Price: $1,295.00. From January 11 to March 4: Regular Price: $1,495.00 Discounts are available for group participation in the following manner: For two attendees: 10% discount For three to six attendees: 20% discount For seven to 10 attendees: 25% discount For more than 10 attendees: 30% discount To avail the above group discounts, all the participants should register by making a single payment. Please note that the registration will be closed two days (48 hours) prior to the start date of the seminar. Call our representative on 1800 447 9407 to have your seats confirmed.

Contact Information:

Event Coordinator Toll free: 1800 447 9407 Fax: 302 288 6884 Email: support@globalcompliancepanel.com Website: https://www.globalcompliancepanel.com LIVE CHAT SUPPORT- http://www.globalcompliancepanel.com/chat/client.php GlobalCompliancePanel NetZealous LLC, 161

Mission Falls Lane

Suite 216, Fremont

CA 94539

Related Articles - Iso 13485 Design, Sox Compliance Training, Design History File, compliance training, Medical Device Training, 510K Compliance Training, 510k Webinar,

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