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Book Synopsis Artificial Intelligence in Medicine by : Niels Peek
Download or read book Artificial Intelligence in Medicine written by Niels Peek and published by Springer. This book was released on 2013-12-06 with total page 334 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book constitutes the refereed proceedings of the 14th Conference on Artificial Intelligence in Medicine, AIME 2013, held in Murcia, Spain, in May/June 2013. The 43 revised full and short papers presented were carefully reviewed and selected from 82 submissions. The papers are organized in the following topical sections: decision support, guidelines and protocols; semantic technology; bioinformatics; machine learning; probabilistic modeling and reasoning; image and signal processing; temporal data visualization and analysis; and natural language processing.
Author :European Federation for Medical Informatics. Conference Publisher :IOS Press ISBN 13 :1614991006 Total Pages :1284 pages Book Rating :4.6/5 (149 download)
Book Synopsis Quality of Life Through Quality of Information by : European Federation for Medical Informatics. Conference
Download or read book Quality of Life Through Quality of Information written by European Federation for Medical Informatics. Conference and published by IOS Press. This book was released on 2012 with total page 1284 pages. Available in PDF, EPUB and Kindle. Book excerpt: Role of e-health in pursuing benefits in terms of quality of life for patients, health-care personnel, citizens and society.
Book Synopsis Pharmacovigilance- An Industry Perspective by : Deepa Arora
Download or read book Pharmacovigilance- An Industry Perspective written by Deepa Arora and published by Pharmapublisher. This book was released on with total page 170 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Stephens' Detection and Evaluation of Adverse Drug Reactions by : John Talbot
Download or read book Stephens' Detection and Evaluation of Adverse Drug Reactions written by John Talbot and published by John Wiley & Sons. This book was released on 2011-12-19 with total page 751 pages. Available in PDF, EPUB and Kindle. Book excerpt: Written with practitioners in mind, this new edition of Stephen’s Detection of Adverse Drug Reactions: Principle and Practice continues to be one of the corner stones of the pharmaceutical medicine list. The classic text covers the issues and problems involved in the detection of adverse drug reactions (ADRs) throughout the life cycle of a medicine from animal studies through to clinical trials, its introduction to the market, followed by wide clinical use, and eventual decline in use or withdrawal. The sixth edition is completely revised and updated including five new chapters on pharmacogenomics, ADRs with herbal medicines, safety of medical devices, safety issues with oncology drugs, and economic aspects of ADRs. All tables and web information needed in order to practice are included to make this sixth edition a complete primer for the new practitioner and a reference for the more experienced.
Book Synopsis Mann's Pharmacovigilance by : Elizabeth B. Andrews
Download or read book Mann's Pharmacovigilance written by Elizabeth B. Andrews and published by John Wiley & Sons. This book was released on 2014-03-24 with total page 878 pages. Available in PDF, EPUB and Kindle. Book excerpt: Highly Commended at the BMA Medical Book Awards 2015 Mann’s Pharmacovigilance is the definitive reference for the science of detection, assessment, understanding and prevention of the adverse effects of medicines, including vaccines and biologics. Pharmacovigilance is increasingly important in improving drug safety for patients and reducing risk within the practice of pharmaceutical medicine. This new third edition covers the regulatory basis and the practice of pharmacovigilance and spontaneous adverse event reporting throughout the world. It examines signal detection and analysis, including the use of population-based databases and pharmacoepidemiological methodologies to proactively monitor for and assess safety signals. It includes chapters on drug safety practice in specific organ classes, special populations and special products, and new developments in the field. From an international team of expert editors and contributors, Mann’s Pharmacovigilance is a reference for everyone working within pharmaceutical companies, contract research organisations and medicine regulatory agencies, and for all researchers and students of pharmaceutical medicine. The book has been renamed in honor of Professor Ronald Mann, whose vision and leadership brought the first two editions into being, and who dedicated his long career to improving the safety and safe use of medicines.
Book Synopsis Side Effects of Drugs Annual by : Jeffrey K. Aronson
Download or read book Side Effects of Drugs Annual written by Jeffrey K. Aronson and published by Elsevier. This book was released on 2009-11-25 with total page 849 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Side Effects of Drugs Annual was first published in 1977. It has been continually published since then, as a yearly update to the voluminous encyclopedia Meyler's Side Effects of Drugs. Each new Annual continues to provide clinicians and medical investigators with a reliable and critical yearly survey of new data and trends in the area of adverse drug reactions and interactions. An international team of specialists has contributed to the informative Annual by critically interpreting it and by pointing to whatever is misleading. Provides a critical yearly survey of new data and trends Special reviews in this Annual include, among other topics: Epidemiology of the use of ecstasy, Paracetamol and the risk of asthma, Combination vaccines/multiple immunizations, Interactions of herbal medicines with warfarin, and Tyrosine kinase inhibitors
Book Synopsis A to Z of Pharmacovigilance by : Dr Azmath Unnisa Begum, VEERENDRA CHAURASIA, Rahathunnisa Begum, Dr. Sarthak Bhattacharya, Meesa Madhavi
Download or read book A to Z of Pharmacovigilance written by Dr Azmath Unnisa Begum, VEERENDRA CHAURASIA, Rahathunnisa Begum, Dr. Sarthak Bhattacharya, Meesa Madhavi and published by Shashwat Publication. This book was released on 2024-04-23 with total page 268 pages. Available in PDF, EPUB and Kindle. Book excerpt: A to Z of Pharmacovigilance serves as your comprehensive companion to understanding the science and practice of drug safety, adhering to the latest syllabus prescribed by the Pharmacy Council of India (BP 805 T). This book empowers pharmacy students and professionals alike to navigate the ever-evolving world of pharmacovigilance. A to Z of Pharmacovigilance is an indispensable resource for Pharmacy students pursuing BP 805 T curriculumand for pharmacy professionals seeking to enhance their pharmacovigilance knowledge and also for anyone who is interested in understanding the importance of drug safety, and want to grasp the global and Indian regulatory framework governing pharmacovigilance activities.
Book Synopsis Drug Safety for Marketed Drugs by : Martin Fagan
Download or read book Drug Safety for Marketed Drugs written by Martin Fagan and published by NetworkPharma Ltd. This book was released on 2006 with total page 24 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Pharmacovigilance Essentials by : Mukesh Nandave
Download or read book Pharmacovigilance Essentials written by Mukesh Nandave and published by Springer Nature. This book was released on with total page 478 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Biopharmaceutical Applied Statistics Symposium by : Karl E. Peace
Download or read book Biopharmaceutical Applied Statistics Symposium written by Karl E. Peace and published by Springer. This book was released on 2018-08-21 with total page 245 pages. Available in PDF, EPUB and Kindle. Book excerpt: This BASS book Series publishes selected high-quality papers reflecting recent advances in the design and biostatistical analysis of biopharmaceutical experiments – particularly biopharmaceutical clinical trials. The papers were selected from invited presentations at the Biopharmaceutical Applied Statistics Symposium (BASS), which was founded by the first Editor in 1994 and has since become the premier international conference in biopharmaceutical statistics. The primary aims of the BASS are: 1) to raise funding to support graduate students in biostatistics programs, and 2) to provide an opportunity for professionals engaged in pharmaceutical drug research and development to share insights into solving the problems they encounter. The BASS book series is initially divided into three volumes addressing: 1) Design of Clinical Trials; 2) Biostatistical Analysis of Clinical Trials; and 3) Pharmaceutical Applications. This book is the second of the 3-volume book series. The topics covered include: Statistical Approaches to the Meta-analysis of Randomized Clinical Trials, Collaborative Targeted Maximum Likelihood Estimation to Assess Causal Effects in Observational Studies, Generalized Tests in Clinical Trials, Discrete Time-to-event and Score-based Methods with Application to Composite Endpoint for Assessing Evidence of Disease Activity-Free , Imputing Missing Data Using a Surrogate Biomarker: Analyzing the Incidence of Endometrial Hyperplasia, Selected Statistical Issues in Patient-reported Outcomes, Network Meta-analysis, Detecting Safety Signals Among Adverse Events in Clinical Trials, Applied Meta-analysis Using R, Treatment of Missing Data in Comparative Effectiveness Research, Causal Estimands: A Common Language for Missing Data, Bayesian Subgroup Analysis with Examples, Statistical Methods in Diagnostic Devices, A Question-Based Approach to the Analysis of Safety Data, Analysis of Two-stage Adaptive Seamless Trial Design, and Multiplicity Problems in Clinical Trials – A Regulatory Perspective.
Book Synopsis Drug Safety Data by : Michael J. Klepper
Download or read book Drug Safety Data written by Michael J. Klepper and published by Jones & Bartlett Learning. This book was released on 2010-10-25 with total page 312 pages. Available in PDF, EPUB and Kindle. Book excerpt: Drug Safety Data: How to Analyze, Summarize and Interpret to Determine Risk was selected for The First Clinical Research Bookshelf - Essential reading for clinical research professionals by the Journal of Clinical Research Best Practices. Drug Safety Data: How to Analyze, Summarize and Interpret to Determine Risk provides drug safety/pharmacovogilance professionals, pharmaceutical and clinical research scientists, statisticians, programmers, medical writers, and technicians with an accessible, practical framework for the analysis, summary and interpretation of drug safety data. The only guide of its kind, Drug Safety Data: How to Analyze, Summarize and Interpret to Determine Risk is an invaluable reference for pre- and post-marketing risk assessment. With decades of pharmaceutical research and drug safety expertise, authors Dr. Klepper and Dr. Cobert discuss how quality planning, safety training, and data standardization result in significant cost, time, and resource savings. Through illustrative, step-by-step instruction, Drug Safety Data: How to Analyze, Summarize and Interpret to Determine Risk is the definitive guide to drug safety data analysis and reporting. Key features include: * Step-by-step instruction on how to analyze, summarize and interpret safety data for mandatory governmental safety reports * Pragmatic tips...and mistakes to avoid * Simple explanations of what safety data are collected, and what the data mean * Practical approaches to determining a drug effect and understanding its clinical significance * Guidance for determining risk throughout the lifecycle of a drug, biologic or nutraceutical * Examples of user-friendly data displays that enhance safety signal identification * Ways to improve data quality and reduce the time, resources and costs involved in mandatory safety reporting * Relevant material for the required training of drug safety/pharmacovigilance professionals * SPECIAL FEATURE: Actual examples of an Integrated Analysis of Safety (IAS) -used in the preparation of the Integrated Summary of Safety (ISS) and the Summary of Clinical Safety (SCS) reports -, and the Periodic Safety Update Report (PSUR)
Book Synopsis Pharmacovigilance (English Edition) by : Dr. Agnimitra Dinda
Download or read book Pharmacovigilance (English Edition) written by Dr. Agnimitra Dinda and published by Thakur Publication Private Limited. This book was released on 2021-03-10 with total page 184 pages. Available in PDF, EPUB and Kindle. Book excerpt: Buy E-Book of Pharmacovigilance (English Edition) Book For B.Pharm 8th Semester of U.P. State Universities
Download or read book SMQs written by Cioms and published by . This book was released on 2004-01-01 with total page 96 pages. Available in PDF, EPUB and Kindle. Book excerpt: The aim of this publication is to brief drug regulatory authorities, scientific institutions and pharmaceutical companies worldwide about the development, purpose and appropriate use of Standardized MedDRA Queries (SMQs) in drug surveillance. Two papers in this publication are to assist in the rational use of search queries in the identification and retrieval of potentially relevant individual case safety reports from a database and to harmonize presentation of search results. It also includes examples to illustrate the structure and content of end product.
Book Synopsis Pharmacovigilance and Pharmacoepidemiology: Public Health and Safety by : Thierry Trenque
Download or read book Pharmacovigilance and Pharmacoepidemiology: Public Health and Safety written by Thierry Trenque and published by Frontiers Media SA. This book was released on 2024-06-24 with total page 190 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacovigilance has historically been based on spontaneous reports. The World Health Organisation (WHO) defines pharmacovigilance as "the science and activities relating to detection, assessment, understanding and prevention of adverse effects or any medicine-related problem" (WHO 2004). Pharmacoepidemiological studies can supplement the role of identification, as the spontaneous reporting of adverse drug reactions and conventional pharmacovigilance, can alert us to other, potentially more major, problems, medicine-related or otherwise.
Book Synopsis Quantitative Drug Safety and Benefit Risk Evaluation by : William Wang
Download or read book Quantitative Drug Safety and Benefit Risk Evaluation written by William Wang and published by CRC Press. This book was released on 2021-12-30 with total page 347 pages. Available in PDF, EPUB and Kindle. Book excerpt: Quantitative Methodologies and Process for Safety Monitoring and Ongoing Benefit Risk Evaluation provides a comprehensive coverage on safety monitoring methodologies, covering both global trends and regional initiatives. Pharmacovigilance has traditionally focused on the handling of individual adverse event reports however recently there had been a shift towards aggregate analysis to better understand the scope of product risks. Written to be accessible not only to statisticians but also to safety scientists with a quantitative interest, this book aims to bridge the gap in knowledge between medical and statistical fields creating a truly multi-disciplinary approach that is very much needed for 21st century safety evaluation.
Book Synopsis Handbook of Personalized Medicine by : Ioannis S. Vizirianakis
Download or read book Handbook of Personalized Medicine written by Ioannis S. Vizirianakis and published by CRC Press. This book was released on 2014-02-12 with total page 1512 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book compiles multidisciplinary efforts to conceptualize the environment in research and clinical setting that creates the fertile ground for the practical utility of personalized medicine decisions and also enables clinical pharmacogenomics for establishing pharmacotyping in drug prescription. Its covers innovative drug formulations and nanot
Book Synopsis Machine Proofs in Geometry by : Shang-Ching Chou
Download or read book Machine Proofs in Geometry written by Shang-Ching Chou and published by World Scientific. This book was released on 1994 with total page 490 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book reports recent major advances in automated reasoning in geometry. The authors have developed a method and implemented a computer program which, for the first time, produces short and readable proofs for hundreds of geometry theorems.The book begins with chapters introducing the method at an elementary level, which are accessible to high school students; latter chapters concentrate on the main theme: the algorithms and computer implementation of the method.This book brings researchers in artificial intelligence, computer science and mathematics to a new research frontier of automated geometry reasoning. In addition, it can be used as a supplementary geometry textbook for students, teachers and geometers. By presenting a systematic way of proving geometry theorems, it makes the learning and teaching of geometry easier and may change the way of geometry education.
