Good Clinical Laboratory Practice Gclp
Download Good Clinical Laboratory Practice Gclp full books in PDF, epub, and Kindle. Read online free Good Clinical Laboratory Practice Gclp ebook anywhere anytime directly on your device. Fast Download speed and no annoying ads. We cannot guarantee that every ebooks is available!
| Author | : Isin Akyar |
| Publisher | : |
| Total Pages | : 546 |
| Release | : 2011 |
| Genre | : |
| ISBN | : 9789535160731 |
Quality control is a standard which certainly has become a style of living. With the improvement of technology every day, we meet new and complicated devices and methods in different fields. Quality control explains the directed use of testing to measure the achievement of a specific standard. It is the process, procedures and authority used to accept or reject all components, drug product containers, closures, in-process materials, packaging material, labeling and drug products, and the authority to review production records to assure that no errors have occurred.The quality which is supposed to be achieved is not a concept which can be controlled by easy, numerical or other means, but it is the control over the intrinsic quality of a test facility and its studies. The aim of this book is to share useful and practical knowledge about quality control in several fields with the people who want to improve their knowledge.
| Author | : |
| Publisher | : |
| Total Pages | : |
| Release | : 2009 |
| Genre | : |
| ISBN | : 9789241597852 |
In 2006, WHO/TDR convened a meeting of organizations engaged in clinical trials in disease endemic countries to discuss the applicability of GCLP guidelines to their work. It was agreed that GCLP would be a valuable tool for improving quality laboratory practice. In line with that agreement, TDR/WHO recently acquired copyright to GCLP guidelines that were originally published in 2003 by a working party of the Clinical Committee of the British Association of Research Quality Assurance (BARQA), with the aim of disseminating them widely in developing countries and developing related training materials. These GCLP guidelines are presented here. Compliance with them will allow clinical laboratories to ensure that safety and efficacy data is repeatable, reliable, auditable and easily reconstructed in a research setting. GCLP guidelines set a standard for compliance by laboratories involved in the analysis of samples from TDR-supported clinical trials.
| Author | : Tim Stiles |
| Publisher | : |
| Total Pages | : 18 |
| Release | : 2003-01-01 |
| Genre | : Clinical trials |
| ISBN | : 9781904610007 |
| Author | : Philip Carson |
| Publisher | : Royal Society of Chemistry |
| Total Pages | : 657 |
| Release | : 2007-10-31 |
| Genre | : Science |
| ISBN | : 1847557724 |
Quality assurance and good laboratory practices are becoming essential knowledge for professionals in all sorts of industries. This includes internal and external audit procedures for compliance with the requirements of good clinical, laboratory and manufacturing practices. Spanning chemical, cosmetic and manufacturing industries, Good Clinical, Laboratory and Manufacturing Practices: Techniques for the QA professional is aimed at: chemists, clinicians, ecotoxicologists, operation managers, pharmaceutical process managers, quality assurance officers, technicians and toxicologists. In addition sections on harmonisation of quality systems will be of value to safety, health and environment advisors. This comprehensive and high level reference will be an indispensable guide to research laboratories in academia and industry. Additional training material is also included.
| Author | : William A. Sollecito |
| Publisher | : Jones & Bartlett Publishers |
| Total Pages | : 644 |
| Release | : 2011-09-01 |
| Genre | : Health & Fitness |
| ISBN | : 1449677487 |
. Through a unique interdisciplinary perspective on quality management in health care, this text covers the subjects of operations management, organizational behavior, and health services research. With a particular focus on Total Quality Management and Continuous Quality Improvement, the challenges of implementation and institutionalization are addressed using examples from a variety of health care organizations, including primary care clinics, hospital laboratories, public health departments, and academic health centers. Important Notice: The digital edition of this book is missing some of the images or content found in the physical edition
| Author | : David Hutchinson |
| Publisher | : |
| Total Pages | : 34 |
| Release | : 2016 |
| Genre | : Clinical trials |
| ISBN | : 9781908278647 |
| Author | : Michael J. McGraw |
| Publisher | : Pharmaceutical Press |
| Total Pages | : 273 |
| Release | : 2010 |
| Genre | : Business & Economics |
| ISBN | : 0853697906 |
Part of "RPS Pharmacy Business Administration Series", this book offers good clinical practice guidelines. It includes standards on how clinical trials should be conducted, provide assurance of safety and efficacy of various drugs and protect human rights.
| Author | : Isin Akyar |
| Publisher | : IntechOpen |
| Total Pages | : 546 |
| Release | : 2011-11-09 |
| Genre | : Technology & Engineering |
| ISBN | : 9789533076836 |
Quality control is a standard which certainly has become a style of living. With the improvement of technology every day, we meet new and complicated devices and methods in different fields. Quality control explains the directed use of testing to measure the achievement of a specific standard. It is the process, procedures and authority used to accept or reject all components, drug product containers, closures, in-process materials, packaging material, labeling and drug products, and the authority to review production records to assure that no errors have occurred.The quality which is supposed to be achieved is not a concept which can be controlled by easy, numerical or other means, but it is the control over the intrinsic quality of a test facility and its studies. The aim of this book is to share useful and practical knowledge about quality control in several fields with the people who want to improve their knowledge.
| Author | : OECD |
| Publisher | : OECD Publishing |
| Total Pages | : 42 |
| Release | : 1999-10-06 |
| Genre | : |
| ISBN | : 9264173706 |
These principles of corporate governance, endorsed by the OECD Council at Ministerial level in 1999, provide guidelines and standards to insure inclusion, accountability and abilit to attract capital.
| Author | : Milica Prostran |
| Publisher | : BoD – Books on Demand |
| Total Pages | : 226 |
| Release | : 2018-05-09 |
| Genre | : Medical |
| ISBN | : 1789232007 |
This book Clinical Trials in Vulnerable Populations has 12 chapters divided into 4 sections: Minority Patients, Women, Medically Compromised Patients and Clinical Trials. Contributing authors came from several countries, from Serbia to Turkey. The book was edited by Professor Milica Prostran MD, Ph.D., specialist in Clinical Pharmacology. The potential reader is shown a modern approach to clinical trials in vulnerable populations, from different points of view. The chapters deal at length and clarity with their topics. Finally, I believe, that this book I edited and reviewed with dedication will capture the attention of many readers, from medical students to practicing doctors and pharmacists. All of whom must consider this very important field of medicine: clinical trials in vulnerable patients.
