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Readers, we are back with one more interesting article—this time with Pharmacovigilance books for reading and spreading knowledge across the globe.
PV Chronicle and team have compiled the top 5 books available online.
The list of 5 books is as follows:
- Evidence-Based Pharmacovigilance: Clinical and Quantitative Aspects (Methods in Pharmacology and Toxicology).
- Cobert’s Manual Of Drug Safety And Pharmacovigilance (Third Edition).
- A Textbook of Clinical Research and Pharmacovigilance.
- Textbook of Pharmacovigilance.
- An Introduction to Pharmacovigilance.
These are the top 5 and best books above the price range of 1000 RS. As you are aware Pharmacovigilance knowledge and insights are always useful for fresher’s and experienced professionals too.
- Evidence-Based Pharmacovigilance: Clinical and Quantitative Aspects (Methods in Pharmacology and Toxicology) :
This book is written by The Quantitative chapters focus more on statistical and epidemiological strategies and the thinking that underpins core developments in Pharmacovigilance. In contrast, 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.
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2. Cobert’s Manual Of Drug Safety And Pharmacovigilance (Third Edition):
Written by Barton Cobert (Author), William Gregory (Author), Jean-loup Thomas (Author)
Completely revised and updated, Cobert’s Manual of Drug Safety and Pharmacovigilance, Third Edition, is a how-to manual for those working in the fields of drug safety, clinical research, pharmacology, regulatory affairs, risk management, quality/compliance, and government and legal professions. This comprehensive and practical guide discusses the theory and the practicalities of drug safety (also known as pharmacovigilance) and provides essential information on drug safety and regulations in the United States, the European Union, and more.
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3. A Textbook of Clinical Research and Pharmacovigilance:
The book is written by the late Dr. KPR Chowdary sir and provides a comprehensive knowledge of various aspects such as drug development and approval process, pharmacological and toxicological approaches and methods, pharmaceutical dosage form approaches for drug development, clinical approaches and clinical trials, phases, types, designs and statistical tests of clinical trials, regulatory aspects, GCP as per ICH, WHO, ICMR, Schedule Y, and regulatory environment in US, Europe, and India in 20 chapters.
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4. Textbook of Pharmacovigilance.
This book is written by SK Gupta PhD DSc FIPS FIACS and Sushma Srivastava PhD PDCR, The Book is an updated second edition of the textbook Pharmacology: ensuring the Safe Use of Medicine. All the chapters have been updated and new chapters like pharmacology and pharmacology, hospitalization due to adverse drug reactions and its economic burden, and vigilance systems for medical devices have been added. This is useful for healthcare professionals, postgraduate students, industry professionals, and those engaged in clinical research in academia and the pharmaceutical industry.
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5. An Introduction to Pharmacovigilance:
Written by Patrick Waller (Author), Mira Harrison-Woolrych. This book is an introductory guide is designed to aid the rapid understanding of the key principles of pharmacovigilance. This is 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.
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