Medical Writing
Medical Writing

Author: Robert B. Taylor

Publisher: Springer Science & Business Media

Published: 2011-08-17

Total Pages: 376

ISBN-13: 1441982345

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The first edition of this book (titled “The Clinician’s Guide to Medical Writing”) has become a standard in its field and remains an indispensible reference for any clinician, academic physician, or health professional who wishes to hone their writing skills. However, since its publication in 2004, significant changes have taken place in the way medical professionals communicate with each other and the world. Medical Writing: A Guide for Clinicians and Academicians, 2e retains all of the fundamental writing advice of the first edition and has been expanded to include two brand new chapters: How to Write a Research Protocol (including why a research project needs a written protocol, elements of the research protocol and common problems) How to Write a Grant Proposal (including sections on government and private grant funding sources, what you need to know about grant writing, and elements of a successful grant proposal) New information is also included throughout the book on becoming a successful writer, medical tables and figures, conflict of interest and disclosures, how to review a scientific article, statistical analysis, “pay-to-publish” journal publishing, electronic submission of manuscripts, issues in medical publishing and the future of medical writing and publication. New appendices address commonly encountered research and statistical terms and memorable aphorisms regarding writing, medical and otherwise.

Clinician's Guide to Medical Writing
Clinician's Guide to Medical Writing

Author: Robert B. Taylor

Publisher: Springer Science & Business Media

Published: 2006-03-20

Total Pages: 270

ISBN-13: 0387270248

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This book is for the clinician who wants to write. It is for the physician, physician assistant, or nurse practitioner who sees patients and who wants to contribute to the medical l- erature. You may be an assistant professor aspiring to p- motion or a clinician in private practice who seeks the personal enrichment that writing can bring. If you are new to medical writing or even if you have been the author of some articles or book chapters and seek to improve your abilities, this book can help you. Who am I that I can make this assertion and write this book, both fairly presumptuous? Here’s my reasoning. As a practicing physician, writing has been my avocation; unlike the authors of many other writing books, I am not a journal editor. Over 14 years in private practice and 26 years in a- demic medicine, I have written all the major models described in this book: review articles, case reports, edito- als, letters to the editor, book reviews, book chapters, edited books, authored books, and reports of clinical research st- ies. Most have been published. Not all. Perhaps my most signi?cant quali?cation is not that I have managed to p- duce a lengthy curriculum vitae. In my opinion, what is more important for you, the reader, is that I have made all the errors. That’s right, the mistakes.

The Complete Guide to Medical Writing
The Complete Guide to Medical Writing

Author: Mark C. Stuart

Publisher: Pharmaceutical Press

Published: 2007

Total Pages: 522

ISBN-13: 9780853696674

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'The Complete Guide to Medical Writing' is intended to consider all aspects of medical/scientific writing in one concise introductory text. It explains how to get published, how to write for a particular audience or in a particular media, what the publishing processes are and what the financial rewards might be.

Pharmacovigilance Medical Writing
Pharmacovigilance Medical Writing

Author: Justina Orleans-Lindsay

Publisher: John Wiley & Sons

Published: 2012-06-22

Total Pages: 182

ISBN-13: 1118302060

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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.

A Field Guide for Science Writers
A Field Guide for Science Writers

Author: Deborah Blum

Publisher: Oxford University Press

Published: 2006

Total Pages: 336

ISBN-13: 0195174992

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This guide offers practical tips on science writing - from investigative reporting to pitching ideas to magazine editors. Some of the best known science witers in the US share their hard earned knowledge on how they do their job.

The Complete Guide to Scientific Manuscript Writing
The Complete Guide to Scientific Manuscript Writing

Author: Andrea R. Gwosdow Ph. D.

Publisher: Aviva Publishing

Published: 2018-11-11

Total Pages: 140

ISBN-13: 9781947937321

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Have you ever wanted to make writing manuscripts easier and more enjoyable? What if you could improve your manuscript writing skills and increase your chances of a favorable review and acceptance for publication? Based on her powerful and much acclaimed manuscript writing course, Dr. Andrea Gwosdow has combined her best practices and proven tools and techniques in The Complete Guide to Scientific Manuscript Writing. You'll find proven guidelines to simplify your writing, scientific pointers for writing each section of your manuscript, a tried and tested format for writing each section of your manuscript, templates, powerful sentence starters, and the best activities and practice exercises to end each chapter.

Medical Writing in Drug Development
Medical Writing in Drug Development

Author: Robert J Bonk

Publisher: Routledge

Published: 2014-01-02

Total Pages: 193

ISBN-13: 1317971418

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A guide through the maze of the pharmaceutical research and development process, Medical Writing in Drug Development fills a gap in the libraries of technical writers, college instructors, and corporate professionals associated with the pharmaceutical process. As it discusses critical information, such as strategies and techniques pivotal to crafting documents for drug development, it also overviews drug research, document types, the roles of professional writers, and information technology. In no time at all, you will be creating persuasive technical documents, building complex facts into coherent messages, and contributing to the effective marketing of new products with promotional pieces that meet legal and ethical standards. Medical Writing in Drug Development helps medical writers and scientific, regulatory, and marketing professionals develop a working knowledge of the technical documents crucial to successful drug research. New and seasoned professional writers alike will benefit from the book's detailed discussions of: using abstracts, slides, and posters to present up-to-the-minute research how patient-education materials, health-economic assessments, and electronic journals provide ongoing challenges in medical writing a dossier approach that expedites regulatory submissions for international drug development structural constraints and rhetorical approaches toward regulatory documents presenting intricate information in scientifically unbiased, yet technically convincing language the effects of electronic publishing, computer graphics, and related technology on the practice of medical writing within pharmaceutical research Practical as a foundation text for undergraduate, graduate, and certificate programs in pharmaceutical or medical technical writing, Medical Writing in Drug Development will help you develop practical strategies for handling journal manuscripts, conference materials, and promotional pieces. No other text will clarify the main aspects of the pharmaceutical research and development process while offering you insight on the key issues dominating the healthcare arena.

Effective Medical Writing: The Write Way To Get Published (UM Press)
Effective Medical Writing: The Write Way To Get Published (UM Press)

Author: Wifred C.G Peh

Publisher: The University of Malaya Press

Published: 2010

Total Pages: 221

ISBN-13: 983100955X

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Effective Medical Writing. The Write Way to get Published was edited and updated from a series of well-received articles published in the Singapore Medical Journal. These articles were used extensively as resource material for numerous medical and scientific writing workshops held in several countries such as Singapore, Malaysia, Thailand, and include the first ever national medical writing workshops staged in The Philippines, Brunei Darussalam, Vietnam, Cambodia and Mongolia, Most of these workshops were endorsed by the Asia Pacific Association of Medical Journal Editors. This book will be helpful to medical and postgraduate students, clinical specialty trainees, aspiring researchers, newly-appointed academic staff, allied health professionals, and those who are looking to write scientific papers and get published. This book is written in an easy-to-read style, covering all the steps required to prepare manuscripts for biomedical and healthcare publications. The reader will learn about “must-know” issues relating to manuscript processing, authoring, reviewing, editing and other key points related to publishing.

Targeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics
Targeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics

Author: Linda Fossati Wood

Publisher: Springer Science & Business Media

Published: 2009-01-05

Total Pages: 235

ISBN-13: 3764383623

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This book describes the authors’ standard or ‘best’ practices used in writing regul- ed clinical documents for the drug and biologics industry. The fundamental premise of this book is that the end (documents submitted to a health authority) is dep- dent on the beginning (the planning and strategy that go into organizing written documentation). Each regulatory document inherently exists within a constellation of related documents. This book attempts to show the relationships between and among these documents and suggests strategies for organizing and writing these documents to maximize ef?ciency while developing clear and concise text. At all times, and irrespective of applicable laws and guidelines, good communication skills and a sense of balance are essential to adequately, accurately, and clearly describe a product’s characteristics. At no time should the reader perceive these suggestions to be the only viable solution to writing regulatory documents nor should the reader expect that these suggestions guarantee product success. The audience for this book is the novice medical writer, or those who would like to explore or enhance regulatory-writing skills. We assume the reader will have a basic understanding of written communication, but little experience in applying this skill to the task of regulatory writing. Extensive knowledge of science, clinical me- cine, mathematics, or regulatory affairs law is not required to use the best practices described in this book.