Good Laboratory Practice Regulations Management Briefings
Author | : United States. Food and Drug Administration |
Publisher | : |
Total Pages | : 60 |
Release | : 1979 |
Genre | : Laboratories |
ISBN | : |
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Author | : United States. Food and Drug Administration |
Publisher | : |
Total Pages | : 60 |
Release | : 1979 |
Genre | : Laboratories |
ISBN | : |
Author | : Sandy Weinberg |
Publisher | : CRC Press |
Total Pages | : 249 |
Release | : 2002-11-06 |
Genre | : Medical |
ISBN | : 0203911083 |
Fully updated and revised to include the latest information since publication of the first edition in 1989, the Second Edition of this highly praised reference covers all aspects of the Food and Drug Administration's (FDA) Good Laboratory Practice (GLP) regulations and techniques for implementation. The book details specific standards and general g
Author | : William J. Brock |
Publisher | : John Wiley & Sons |
Total Pages | : 568 |
Release | : 2014-06-03 |
Genre | : Science |
ISBN | : 1118370392 |
A single-source reference with a broad and holistic overview of nonclinical studies, this book offers critical training material and describes regulations of nonclinical testing through guidelines, models, case studies, practical examples, and worldwide perspectives. The book: Provides a complete overview of nonclinical study organization, conduct, and reporting and describes the roles and responsibilities of a Study Director to manage an effective study Covers regulatory and scientific concepts, including international testing and Good Laboratory Practice (GLP), compliance with guidelines, and animal models Features a concluding chapter that compiles case studies / lessons learned from those that have served as a Study Director for many years Addresses the entire spectrum of nonclinical testing, making it applicable to those in the government, laboratories and those actively involved in in all sectors of industry
Author | : Allen F. Hirsch |
Publisher | : Marcel Dekker |
Total Pages | : 248 |
Release | : 1989 |
Genre | : Medical |
ISBN | : |
Author | : World Health Organization |
Publisher | : |
Total Pages | : 0 |
Release | : 2011 |
Genre | : Laboratories |
ISBN | : 9789241548274 |
Achieving, maintaining and improving accuracy, timeliness and reliability are major challenges for health laboratories. Countries worldwide committed themselves to build national capacities for the detection of, and response to, public health events of international concern when they decided to engage in the International Health Regulations implementation process. Only sound management of quality in health laboratories will enable countries to produce test results that the international community will trust in cases of international emergency. This handbook was developed through collaboration between the WHO Lyon Office for National Epidemic Preparedness and Response, the United States of America Centers for Disease Control and Prevention (CDC) Division of Laboratory Systems, and the Clinical and Laboratory Standards Institute (CLSI). It is based on training sessions and modules provided by the CDC and WHO in more than 25 countries, and on guidelines for implementation of ISO 15189 in diagnostic laboratories, developed by CLSI. This handbook is intended to provide a comprehensive reference on Laboratory Quality Management System for all stakeholders in health laboratory processes, from management, to administration, to bench-work laboratorians. This handbook covers topics that are essential for quality management of a public health or clinical laboratory. They are based on both ISO 15189 and CLSI GP26-A3 documents. Each topic is discussed in a separate chapter. The chapters follow the framework developed by CLSI and are organized as the "12 Quality System Essentials".
Author | : William J. Brock |
Publisher | : John Wiley & Sons |
Total Pages | : 568 |
Release | : 2014-05-02 |
Genre | : Science |
ISBN | : 1118874080 |
A single-source reference with a broad and holistic overview of nonclinical studies, this book offers critical training material and describes regulations of nonclinical testing through guidelines, models, case studies, practical examples, and worldwide perspectives. The book: Provides a complete overview of nonclinical study organization, conduct, and reporting and describes the roles and responsibilities of a Study Director to manage an effective study Covers regulatory and scientific concepts, including international testing and Good Laboratory Practice (GLP), compliance with guidelines, and animal models Features a concluding chapter that compiles case studies / lessons learned from those that have served as a Study Director for many years Addresses the entire spectrum of nonclinical testing, making it applicable to those in the government, laboratories and those actively involved in in all sectors of industry
Author | : Adil E. Shamoo |
Publisher | : Taylor & Francis |
Total Pages | : 196 |
Release | : 1989 |
Genre | : Business & Economics |
ISBN | : 9782881243783 |
First published in 1989. Routledge is an imprint of Taylor & Francis, an informa company.
Author | : Ahmed Badr Eldin |
Publisher | : BoD – Books on Demand |
Total Pages | : 554 |
Release | : 2011-11-09 |
Genre | : Technology & Engineering |
ISBN | : 9533079711 |
Rapid advance have been made in the last decade in the quality control procedures and techniques, most of the existing books try to cover specific techniques with all of their details. The aim of this book is to demonstrate quality control processes in a variety of areas, ranging from pharmaceutical and medical fields to construction engineering and data quality. A wide range of techniques and procedures have been covered.
Author | : Carmen Medina |
Publisher | : CRC Press |
Total Pages | : 604 |
Release | : 2003-12-09 |
Genre | : Medical |
ISBN | : 1135520461 |
This text lists the necessary steps for meeting compliance requirements during the drug development process. It presents comprehensive approaches for validating analytical methods for pharmaceutical applications.
Author | : Sandy Weinberg |
Publisher | : CRC Press |
Total Pages | : 160 |
Release | : 2007-01-19 |
Genre | : Medical |
ISBN | : 104016689X |
Recent changes in the interpretation and enforcement of 21 CFR Part 11 have shifted the focus of Good Laboratory Practice (GLP) regulations to concentrate on the acceptance of electronic signatures, the archiving of data, the security of electronic documents, and the automation of laboratory procedures. This all-encompassing Fourth Edition addresse