EBookClubs

Read Books & Download eBooks Full Online

EBookClubs

Read Books & Download eBooks Full Online

Book Practical Drug Safety from A to Z

Download or read book Practical Drug Safety from A to Z written by Barton Cobert and published by Jones & Bartlett Publishers. This book was released on 2009-10-06 with total page 406 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Practical Drug Safety from A to Z is an alphabetical guide to drug safety monitoring (pharmacovigilance), covering literally, the "A to Z" of maintaining drug safety. Written by experts in the field, this book is a perfect to companion to the Manual of Drug Safety and Pharmacovigilance and an essential reference for pharmacists, pharmacologists, hospital administrators, medical liability lawyers, and others.

Book An Introduction to Pharmacovigilance

Download or read book An Introduction to Pharmacovigilance written by Patrick Waller and published by John Wiley & Sons. This book was released on 2017-02-14 with total page 192 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. This introductory guide is designed to aid the rapid understanding of the key principles of pharmacovigilance. Packed full of examples illustrating drug safety issues it not only covers the processes involved, but the regulatory aspects and ethical and societal considerations of pharmacovigilance. Covering the basics step-by-step, this book is perfect for beginners and is essential reading for those new to drug safety departments and pharmaceutical medicine students. The second edition is thoroughly revised and updated throughout and includes a new chapter on clinical aspects of pharmacovigilance.

Book Pharmaco Vigilance from A to Z

Download or read book Pharmaco Vigilance from A to Z written by Barton L. Cobert, MD and published by Wiley-Blackwell. This book was released on 2001-07-05 with total page 252 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacovigilance from A to Z is an authoritative text focusing on the common questions and procedures involved in prescribed-drug monitoring. The alphabetized format provides an easy-to-use reference, while a separate section of the book guides the reader logically from topic to topic to form related "chapters."

Book Pharmacovigilance

    Book Details:
  • Author : Charmy S. Kothari
  • Publisher : BoD – Books on Demand
  • Release : 2019-03-20
  • ISBN : 1789857597
  • Pages : 90 pages

Download or read book Pharmacovigilance written by Charmy S. Kothari and published by BoD – Books on Demand. This book was released on 2019-03-20 with total page 90 pages. Available in PDF, EPUB and Kindle. Book excerpt: The book "Pharmacovigilance" describes the pathway to understand that pharmacovigilance plays a specialized and pivotal role in ensuring ongoing safety of medicinal products. Written in plain English, the book is concise, jargon-free, and facilitates an understanding of fundamentals of pharmacovigilance and explores regulatory aspects involved in pharmacovigilance.

Book Cobert s Manual of Drug Safety and Pharmacovigilance

Download or read book Cobert s Manual of Drug Safety and Pharmacovigilance written by Barton Cobert and published by Jones & Bartlett Publishers. This book was released on 2011-04 with total page 431 pages. Available in PDF, EPUB and Kindle. Book excerpt: Completely revised and updated, the Manual of Drug Safety and Pharmacovigilance, Second Edition is a how-to manual for those working in the fields of drug safety, clinical research, pharmacuetucal, regulatory affairs, government and legal professions. This comprehensive and practical guide discusses the theory and the practicalities of drug safety (also known as pharmacovigilance) and side effects, as well as providing essential information on drug safety and regulations, including: recognizing, monitoring, reporting, and cataloging serious adverse drug reactions. The Manual of Drug Safety and Pharmacovigilance, Second Edition teaches the ins and outs of drug safety in the industry, hospitals, FDA, and other health agencies both in the US and around the world, and presents critical information about what is done when confronted with a drug safety problem.

Book Drug Safety Data

    Book Details:
  • Author : Michael J. Klepper
  • Publisher : Jones & Bartlett Learning
  • Release : 2011
  • ISBN : 0763769126
  • Pages : 332 pages

Download or read book Drug Safety Data written by Michael J. Klepper and published by Jones & Bartlett Learning. This book was released on 2011 with total page 332 pages. Available in PDF, EPUB and Kindle. Book excerpt: Drug Safety Data: How to Analyze, Summarize and Interpret to Determine Risk provides pharmaceutical scientists, researchers 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 premarketing risk assessment. This unique resource enhances the ability of pharmaceutical professionalsùthose with and without clinical trainingùto determine the risk of a drug or biologic­ ahead of its release, thereby reducing unnecessary jeopardy to the patient. Authors Dr. Michael Klepper and Dr. Barton Cobert, who together bring decades of pharmaceutical research and drug safety expertise, 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 provides 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 tipsàand 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 An Introduction to Pharmacovigilance

Download or read book An Introduction to Pharmacovigilance written by Patrick Waller and published by John Wiley & Sons. This book was released on 2017-05-01 with total page 194 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. This introductory guide is designed to aid the rapid understanding of the key principles of pharmacovigilance. Packed full of examples illustrating drug safety issues it not only covers the processes involved, but the regulatory aspects and ethical and societal considerations of pharmacovigilance. Covering the basics step-by-step, this book is perfect for beginners and is essential reading for those new to drug safety departments and pharmaceutical medicine students. The second edition is thoroughly revised and updated throughout and includes a new chapter on clinical aspects of pharmacovigilance.

Book Practical Drug Safety from A to Z  9780763745271

Download or read book Practical Drug Safety from A to Z 9780763745271 written by Cobert and published by . This book was released on 2009 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book A to Z of Pharmacovigilance

    Book Details:
  • Author : Dr Azmath Unnisa Begum, VEERENDRA CHAURASIA, Rahathunnisa Begum, Dr. Sarthak Bhattacharya, Meesa Madhavi
  • Publisher : Shashwat Publication
  • Release : 2024-04-23
  • ISBN : 9360870366
  • Pages : 268 pages

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 Pharmacovigilance Medical Writing

Download or read book Pharmacovigilance Medical Writing written by Justina Orleans-Lindsay and published by John Wiley & Sons. This book was released on 2012-06-22 with total page 182 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e.g. scheduling, source data, department/functions involved in document preparation/review, appropriate timelines and planning activities), ending with a generic model document compliant with the current guidelines, which can be modified to meet specific company and product requirements.

Book Pharmacovigilance  An Industry Perspective

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 Pharmacovigilance  A Practical Approach

Download or read book Pharmacovigilance A Practical Approach written by Thao Doan and published by Elsevier Health Sciences. This book was released on 2018-07-31 with total page 228 pages. Available in PDF, EPUB and Kindle. Book excerpt: Written by experts in the field of pharmacovigilance and patient safety, this concise resource provides a succinct, easy-to-digest overview of an increasingly critical area of medical safety. Drs. Thao Doan, Fabio Lievano, Mondira Bhattacharya, and Linda Scarazzini provide essential information for health care professionals, clinical researchers, and regulators who need a comprehensive, up-to-date source of information on the principles and practice of pharmacovigilance.

Book Evidence Based Pharmacovigilance

Download or read book Evidence Based Pharmacovigilance written by Andrew Bate and published by Humana. This book was released on 2018-10-26 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book examines insights into the latest thinking and core concepts in areas of key methodological endeavor in Pharmacovigilance (PV), which strives to ever more effectively protect patients from harm caused by the medicines they need. Each book chapter tends to have a clear quantitative or clinical slant and an aim to provide an overview of methodological insights within a specific topic, while also providing a perspective on how the area is anticipated to develop in the future. Quantitative chapters focus more on statistical and epidemiological strategies and the thinking that underpins core developments in Pharmacovigilance, whereas clinical chapters focus on clinical methods for detecting hypotheses for and determining side effects of medicinal products as well as misdiagnosis pitfalls. Examples of areas of importance include signal detection, risk management, and risk benefit assessment. Vital and authoritative, Evidence-Based Pharmacovigilance: Clinical and Quantitative Aspects aims to provide readers with a sense of the advances that have occurred in pharmacovigilance methods and approaches, as well as inspiration and motivation to advance the field of pharmacovigilance with a strong sense that there is much more work to be done in ensuring the safe use of medications by patients.

Book Dictionary of Pharmacovigilance

Download or read book Dictionary of Pharmacovigilance written by Amer Alghabban and published by . This book was released on 2004 with total page 527 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Book Pharmacovigilance Made Easy

Download or read book Pharmacovigilance Made Easy written by Gopala Krishna Varshith and published by . This book was released on with total page 160 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmacovigilance Made Easy is a compilation of all the material which is essential to understand and practice the concepts of Pharmacovigilance and Patient Safety for Freshers who wish to swim on the surface as well as for Experienced Professional's who wishes to dive deeper. It also contains a compilation of the most frequently asked interview questions in the domain of Pharmacovigilance.

Book A Magnificient Text Book Of Pharmacovigillance

Download or read book A Magnificient Text Book Of Pharmacovigillance written by ZAKIR HUSSAIN and published by Orangebooks Publication. This book was released on 2019-12-28 with total page 106 pages. Available in PDF, EPUB and Kindle. Book excerpt: A Magnificent text book of pharmacovigillance (post marketing surveillance) is most demanded and recommended text book now a days as the material provided in this book is gathered from different universities framed in their curriculum accordingly we prepared the manuscript to reach the customer demand more over it provides a brief history and background of pharmacovigillance the student can easy understand the language and score good marks in their exam the present books available in market either provide with less information or not upto the bench mark. I have tried my level best to provide the maximum information for the betterment of student and accademic faculties.

Book Mann s Pharmacovigilance

    Book Details:
  • Author : Elizabeth B. Andrews
  • Publisher : John Wiley & Sons
  • Release : 2014-03-24
  • ISBN : 1118820142
  • Pages : 878 pages

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.