An Algorithm For Determining Bayesian Attribute Single Sampling Acceptance Plans PDF Download

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A Bayesian Analysis for Economic Design of Single Sampling Plans for a Sequence of Lots

A Bayesian Analysis for Economic Design of Single Sampling Plans for a Sequence of Lots
Author: Fernando L. Taracena
Publisher:
Total Pages: 226
Release: 1983
Genre: Acceptance sampling
ISBN:

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A dynamic approach to the Bayesian theory of sampling inspection by attributes for the single sampling case is presented. A model is developed which assumes a sequence of lots of equal known size and lots generated by a process operating in a random manner. The model also assumes constant associated costs for all lots and that the posterior distribution of the process quality of a given lot becomes the prior distribution of the process quality of the next lot. This allows the information from one lot to be used in the decision making for subsequent lots. The model is formulated by using a mixed binomial distribution with beta weights as the prior distribution of the lot quality. An improved algorithm for the solution of the single lot case, bounds for the optimal sample size, a lower bound for the expected cost of sampling for the single lot case and a lower bound for the expected cost for the sequence of lots are presented. Optimality conditions for the non-sampling alternatives, the 100% sampling case, and the convergence of the optimal acceptance plan when the number of lots in the sequence tends to infinity are investigated. The model is formulated as a dynamic programming problem with sampling, reject without sampling and accept without sampling as the possible actions; and the lots as the stages. Relationships between the optimal actions at different lots which are independent of the form of the expected cost of sampling function are presented. Exact and approximate solution algorithms are developed and tested. Experimental results indicate that the use of the bounds for the optimal sample size, the lower bound for the expected cost of sampling and the results on optimality of the non-sampling alternatives lead to the pruning of a large part of the decision tree. Approximate methods developed can be classified as forward-back ward procedures. The forward pass reduces the state space by fixing the sample size for all lots but the last one, according to a specified set of rules. The backward pass uses the dynamic programming formulation for finding the optimal policy for the reduced state space. The effectiveness of the approximate methods were evaluated in terms of the quality of the solutions and the computational effort to obtain the solutions. Results indicate that efficiency of two of the approximate methods is very high while computational requirements are drastically reduced.


Encyclopedia of Biopharmaceutical Statistics - Four Volume Set

Encyclopedia of Biopharmaceutical Statistics - Four Volume Set
Author: Shein-Chung Chow
Publisher: CRC Press
Total Pages: 2434
Release: 2018-09-03
Genre: Medical
ISBN: 1351110268

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Since the publication of the first edition in 2000, there has been an explosive growth of literature in biopharmaceutical research and development of new medicines. This encyclopedia (1) provides a comprehensive and unified presentation of designs and analyses used at different stages of the drug development process, (2) gives a well-balanced summary of current regulatory requirements, and (3) describes recently developed statistical methods in the pharmaceutical sciences. Features of the Fourth Edition: 1. 78 new and revised entries have been added for a total of 308 chapters and a fourth volume has been added to encompass the increased number of chapters. 2. Revised and updated entries reflect changes and recent developments in regulatory requirements for the drug review/approval process and statistical designs and methodologies. 3. Additional topics include multiple-stage adaptive trial design in clinical research, translational medicine, design and analysis of biosimilar drug development, big data analytics, and real world evidence for clinical research and development. 4. A table of contents organized by stages of biopharmaceutical development provides easy access to relevant topics. About the Editor: Shein-Chung Chow, Ph.D. is currently an Associate Director, Office of Biostatistics, U.S. Food and Drug Administration (FDA). Dr. Chow is an Adjunct Professor at Duke University School of Medicine, as well as Adjunct Professor at Duke-NUS, Singapore and North Carolina State University. Dr. Chow is the Editor-in-Chief of the Journal of Biopharmaceutical Statistics and the Chapman & Hall/CRC Biostatistics Book Series and the author of 28 books and over 300 methodology papers. He was elected Fellow of the American Statistical Association in 1995.


How and when to Perform Bayesian Acceptance Sampling

How and when to Perform Bayesian Acceptance Sampling
Author: Thomas W. Calvin
Publisher: Asq Corporation
Total Pages: 32
Release: 1990
Genre: Business & Economics
ISBN:

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This how-to book gives a clear rationale for the use of Bayesian methods by comparing them with conventional acceptance sampling approaches.Contents:Introduction to Bayesian Acceptance Sampling Bayesian Acceptance Sampling Distributions Examples of Plan Section