Good Informatics Practices (GIP) Module: Data Management

Good Informatics Practices (GIP) Module: Data Management PDF Author: Robert Barr
Publisher: HIMSS
ISBN:
Category :
Languages : en
Pages : 92

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Book Description

Good Informatics Practices (GIP) Module: Data Management

Good Informatics Practices (GIP) Module: Data Management PDF Author: Robert Barr
Publisher: HIMSS
ISBN:
Category :
Languages : en
Pages : 92

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Book Description


Good Informatics Practices (GIP) Module: Risk Management

Good Informatics Practices (GIP) Module: Risk Management PDF Author: Ford Winslow, Roger Fraumann, CISSP, Robert Sturm, MBA, DeEtte Trubey, PMP
Publisher: HIMSS
ISBN:
Category :
Languages : en
Pages : 128

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Book Description


Good Informatics Practices (GIP) Module: Security

Good Informatics Practices (GIP) Module: Security PDF Author: Michael Cox, CIPP, Tom Czwornog, Roger Fraumann, CISSP, Oscar Ghopeh, PMP, CSM, David Spellmeyer, DeEtte Trubey, PMP, Ford Winslow
Publisher: HIMSS
ISBN:
Category :
Languages : en
Pages : 111

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Book Description


Good Informatics Practices (GIP) Module: Infrastructure and Cloud

Good Informatics Practices (GIP) Module: Infrastructure and Cloud PDF Author: Jeffrey Guo
Publisher: HIMSS
ISBN:
Category :
Languages : en
Pages : 90

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Book Description


Good Informatics Practices (GIP) Module: Training and Training Practices

Good Informatics Practices (GIP) Module: Training and Training Practices PDF Author: Heidi Bargerhuff
Publisher: HIMSS
ISBN:
Category :
Languages : en
Pages : 120

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Book Description


Good Informatics Practices (GIP) Module: Validation & Verification

Good Informatics Practices (GIP) Module: Validation & Verification PDF Author: Frank Cicero, PMP
Publisher: HIMSS
ISBN:
Category : Medical care
Languages : en
Pages : 248

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Book Description


Good Informatics Practices (GIP) Guidance: Introduction and Intended Use

Good Informatics Practices (GIP) Guidance: Introduction and Intended Use PDF Author: Healthcare Information and Management Systems Society (HIMSS)
Publisher: HIMSS
ISBN:
Category :
Languages : en
Pages : 8

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Book Description


Clinical Decision Support System

Clinical Decision Support System PDF Author: Fouad Sabry
Publisher: One Billion Knowledgeable
ISBN:
Category : Computers
Languages : en
Pages : 138

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Book Description
What Is Clinical Decision Support System A clinical decision support system, often known as a CDSS, is a type of health information technology that offers physicians, staff members, patients, and other individuals access to knowledge and information that is personal to them in order to improve health and health care. The Clinical Decision Support System (CDSS) is comprised of several different applications that improve clinical workflow decision-making. These tools include computerized alerts and reminders to care providers and patients, clinical guidelines, condition-specific order sets, focused patient data reports and summaries, documentation templates, diagnostic support, and contextually appropriate reference information, as well as a variety of other tools. A working definition of "health evidence" has been offered by Robert Hayward of the Centre. It reads as follows: "Clinical decision support systems link health observations with health knowledge to influence health choices by clinicians for improved health care." CDSSs comprise a prominent topic in artificial intelligence in medicine. How You Will Benefit (I) Insights, and validations about the following topics: Chapter 1: Clinical decision support system Chapter 2: Gello Expression Language Chapter 3: International Health Terminology Standards Development Organisation Chapter 4: Medical algorithm Chapter 5: Health informatics Chapter 6: Personal Health Information Protection Act Chapter 7: Treatment decision support Chapter 8: Artificial intelligence in healthcare Chapter 9: Health information technology Chapter 10: Applications of artificial intelligence (II) Answering the public top questions about clinical decision support system. (III) Real world examples for the usage of clinical decision support system in many fields. (IV) 17 appendices to explain, briefly, 266 emerging technologies in each industry to have 360-degree full understanding of clinical decision support system' technologies. Who This Book Is For Professionals, undergraduate and graduate students, enthusiasts, hobbyists, and those who want to go beyond basic knowledge or information for any kind of clinical decision support system.

Scientific and Technical Acronyms, Symbols, and Abbreviations

Scientific and Technical Acronyms, Symbols, and Abbreviations PDF Author: Uwe Erb
Publisher: Wiley-Interscience
ISBN:
Category : Language Arts & Disciplines
Languages : en
Pages : 2136

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Book Description
With 200,000 entries in over eighty different fields, Scientific and Technical Acronyms, Symbols, and Abbreviations is the most comprehensive reference of its type, covering more scientific and technical disciplines than any other available book. This invaluable resource will help scientists, engineers, and researchers understand and utilize current terminology in almost any field-from aeronautics to zoology. All accepted abbreviations, acronyms, and symbols are included, from the most obscure to the most common, as well as an appendix that provides important lists of units, systems of units, conversion factors, and prefixes. Science writers, journalists, translators, interpreters-anyone working in or around the sciences-will find this a helpful, easy-to-use guide to difficult technical jargon. Entries are listed in alphabetical order and are defined according to the field in which they are currently in use. Multiple definitions are listed for abbreviations and acronyms that may be in use in more than one field. For instance, the entry for the abbreviation "cb" would show several meanings: "CB" for Canada Balsam, "Cb" for cerebellum, and "c-B" for crystalline boron, among others. Entries for terms in languages other than English are included, as well as abbreviations for all known scientific and technical journals. Simple, comprehensive, and up-to-date, Scientific and Technical Acronyms, Symbols, and Abbreviations is a complete and vital reference for professionals in almost any scientific or technical discipline.

Guide to EU and UK Pharmaceutical Regulatory Law

Guide to EU and UK Pharmaceutical Regulatory Law PDF Author: Sally Shorthose
Publisher: Kluwer Law International B.V.
ISBN: 9403530235
Category : Law
Languages : en
Pages : 840

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Book Description
In the European Union (EU), its Member States and the United Kingdom (UK) post-Brexit, as elsewhere, the marketing of pharmaceuticals is subject to an ever more complex web of legislation and regulation, resulting from the intense scrutiny necessary to ensure such essential products are not only efficacious but also safe. This useful volume lays out this system with extraordinary clarity and logic. Adopting a Europe-wide perspective on the law governing pharmaceuticals, expert authors from the law firm Bird & Bird LLP map the life cycle of a medicinal product or medical device from development to clinical trials to product launch and ongoing pharmacovigilance, offering comprehensive and unambiguous guidance at every stage. Following a brief overview of how the exit from the EU by the UK currently affects the regulatory regime, as well as an introductory overview focusing on the regulatory framework for pharmaceuticals in Europe – from its underlying rationales to the relevant committees and agencies – each of the following twenty-one incisive chapters examines a particular process or subject. Among the many topics and issues covered from both an EU and UK perspective are the following: clinical trials; stages and standards for creating a product dossier; obtaining a marketing authorisation; how and when an abridged marketing authorisation procedure can be used; criteria for conditional marketing authorisations; generic products and ‘essential similarity’; paediatric use and the requisite additional trials; orphan medicinal products; biologicals and ‘biosimilars’; homeopathic, herbal and similar medicines; medical devices; pandemics, epidemics and vaccines; pharmacovigilance; parallel trade; advertising; and relevant competition law, intellectual property rights and data protection regulation. In addition, sample forms and URLs for the most important reference materials are included. Pharmaceutical lawyers and regulatory advisers, both in-house and in private practice, will welcome this unique book. It offers immeasurable value for all who need to understand the process of bringing a medicinal product or medical device to market and the continuing rights and obligations.