Principles good clinical practice (26 resultados)
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Librería: Goodwill of Silicon Valley, SAN JOSE, CA, Estados Unidos de AmericaGoodwill of Silicon Valley
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Condición: good. Supports Goodwill of Silicon Valley job training programs. The cover and pages are in Good condition! Any other included accessories are also in Good condition showing use. Use can include some highlighting and writing, page and cover creases as well as other types visible wear.
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Librería: California Books, Miami, FL, Estados Unidos de AmericaCalifornia Books
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Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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Paperback. Condición: Brand New. reprint edition. 212 pages. 8.43x5.85x0.73 inches. In Stock.
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Librería: GreatBookPricesUK, Woodford Green, Reino UnidoGreatBookPricesUK
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Librería: GreatBookPricesUK, Woodford Green, Reino UnidoGreatBookPricesUK
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Condición: New. 2017. Paperback. . . . . . Books ship from the US and Ireland.
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Librería: AHA-BUCH GmbH, Einbeck, AlemaniaAHA-BUCH GmbH
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EUR 24,77
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Taschenbuch. Condición: Neu. Druck auf Anfrage Neuware - Printed after ordering - Establishing ethical and privacy protection aspects in scientific research, especially in medical research, has a long history. Medical data are usually more sensible than other personal data and require therefore an even higher degree of protectio…n than other personal data. In recent research projects genetic evaluations become more and more important and trigger thereby new and continuing activities in the context of data protection. Genetic data as a subset of medical data are the most sensible category of personal data and require therefore the highest degree of data protection.The book provides a systematic and itemized approach to data protection in clinical research including the handling of genetic material, genetic samples as well as derived genetic data and the subsequent secure storage of them. The set up of different kinds of clinical trials having in addition a genetic part, the concept of a genetic informed consent as well as collection schemes of samples are described in detail. Technical requirements and aspects of data protection including pseudonymization and anonymization procedures taking into account ethics committees requirements as well as the underlying legal framework are also presented.Without any exception, all principles and methods presented are best practices, repeatedly applied in different clinical environments and by no means theoretical considerations.
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- Primera edición
Librería: killarneybooks, Inagh, CLARE, Irlandakillarneybooks
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EUR 56,52
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Hardcover. Condición: Near Fine. 1st Edition. Hardcover, xii + 198 pages, NOT ex-library. A clean and bright copy with unmarked text and firm binding, free of inscriptions and stamps. Boards show mild handling wear. Issued without a dust jacket. -- Contents: 1 Introduction 2 Study Modes [Screening Mode: Pharmacogenetic Informati…on for Screening;Pre- Unspecified Mode: Pharmacogenetic as Part of a Study; Possible Approaches, Summary: Clinical Trial with Genetic Part; Biobanks: What do we Mean by That?] 3 Protection Masks & Procedures [Identified Samples/Data; De-identified Samples/Data; Anonymized Samples/Data; Re-identification] 4 Coding Methods for De-identified Samples/Data [Single & Double & Triple-coded Samples/Data] 5 Relationships Among the Protection Masks 6 Data Types 7 Anonymization [Basic Terms & Ideas; Masking; Discarding the Key; Maintaining the Reliability of Stored Data; Security Measures] 8 Validation: A Brief Introduction [Preliminaries; Basic Definitions & Terms; General Principles of Computer System Validation; Primary Validation: Specification Phase & Preparing Operational Use & Testing Phase] 9 Request Management [Genetic Review Board (GRB); Request Specification; Subrequest Specification; Involvement of External Service Providers] 10 Legal Requirements & Regulations [Basic Ideas; Data Protection in the European Union (EU); Transfer of Personal Data to Third Countries; Binding Corporate Rules; Data Protection in the United States (U.S.): A Brief History] 11 Informed Consent [Sections Mandatory for a Genetic Informed Consent] 12 Selected Data Protection & Medical Sites [Germany; Europe; US; Global Initiatives] 13 Impact of External Services on Data Protection [Introduction; Scenario 1: Using GDI Throughout; Scenario 2: Replacing GDI by nGDI Upon Sample Registration, Performed by regCRO; Scenario 3: Replacing GDI by nGDI Upon Sample Registration, Performed by Sponsor; Scenario 4: Sample Registration by CRO, Proprietary Labeling with CROSID; Scenario 5: Barcoded Label bSID at Study Site; Overall Summary; External Statistical Evaluation; External Biobanking] 14 Practical Approach to Clinical Trials with Supplementary Genetic Parts [Introduction; Overall Project Topology; Checklist: Trial Set-up & System Topology & Sample Management & ICs, Ethics Committees Restrictions & Anonymization & Statistical Evaluation] 15 Appendix 1: Data Protection in the European Union [Council of Europe (COE); EU Privacy Directive: Definitions; Tasks of the Article 29 Data Protection Working Party] 16 Appendix 2: Data types [EU Privacy Directive (October 24,1995); Council of Europe (COE) Definition of Data Types; Federal Data Protection Act (GER) as of 1. Jan. 2003] 17 Appendix 3: Protection Masks [EMA definition of anonymous sample/data; Germany; Spain; US] 18 Appendix4: Informed Consent (IC) [Nuremberg Code; EU Privacy Directive (October 24,1995); COE: Rec No. R (97) 5, Explanatory Memorandum to Rec (97) 5; Oviedo Convention; UNESCO Universal Declaration on Bioethics & Human Rights; Key Issues in Informed Consent for Pharmacogenomics Research; International Declaration On Human Genetic Data; CIOMS: Ethical Guidelines for Biomedical Research; Human Genetic Examination Act (Genetic Diagnosis Act Gen DG)] 19 Appendix 5: Security [EU Privacy Directive (October 24,1995); Federal Data Protection Act (Germany); Council of Europe Recommendation No. R (97) 5; US: Privacy Act of 1974 (Comments from William W. Lowrance, cf. (42)); Safe Harbor Privacy Principles 2000; UN: ICCPR International Covenant on Civil & Political Rights] 20 Abbreviations 21 References; Index -- The book provides a systematic and itemized approach to data protection in clinical research including the handling of genetic material, genetic samples as well as derived genetic data and the subsequent secure storage of them. The set up of different kinds of clinical trials having in addition a genetic part, the concept of a genetic informed consent as well as collection schemes of samples are described in detail.
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Librería: preigu, Osnabrück, Alemaniapreigu
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EUR 22,10
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Taschenbuch. Condición: Neu. G3P - Good Privacy Protection Practice in Clinical Research | Principles of Pseudonymization and Anonymization | Markus Schröder (u. a.) | Taschenbuch | Einband - flex.(Paperback) | Englisch | 2017 | De Gruyter | EAN 9783110554366 | Verantwortliche Person für die EU: De Gruyter [9], Genthiner Str. 13…, 10785 Berlin, orders[at]degruyter[dot]com | Anbieter: preigu.
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Librería: Anybook.com, Lincoln, Reino UnidoAnybook.com
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EUR 113,99
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Condición: Fair. This is an ex-library book and may have the usual library/used-book markings inside.This book has soft covers. In fair condition, suitable as a study copy. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,500grams, ISBN:9780853697909.
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Librería: Ria Christie Collections, Uxbridge, Reino UnidoRia Christie Collections
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Librería: GreatBookPricesUK, Woodford Green, Reino UnidoGreatBookPricesUK
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Librería: GreatBookPrices, Columbia, MD, Estados Unidos de AmericaGreatBookPrices
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EUR 201,71
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Librería: GreatBookPricesUK, Woodford Green, Reino UnidoGreatBookPricesUK
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EUR 203,12
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Librería: California Books, Miami, FL, Estados Unidos de AmericaCalifornia Books
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EUR 222,34
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Librería: Buchpark, Trebbin, AlemaniaBuchpark
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EUR 130,09
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Condición: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher | Establishing ethical and privacy protection aspects in scientific research, especially in medical research, has a long history. Medical data are usually more sensible than other personal data and require therefore an even higher degree of protectio…n than other personal data. In recent research projects genetic evaluations become more and more important and trigger thereby new and continuing activities in the context of data protection. Genetic data as a subset of medical data are the most sensible category of personal data and require therefore the highest degree of data protection. The book provides a systematic and itemized approach to data protection in clinical research including the handling of genetic material, genetic samples as well as derived genetic data and the subsequent secure storage of them. The set up of different kinds of clinical trials having in addition a genetic part, the concept of a genetic informed consent as well as collection schemes of samples are described in detail. Technical requirements and aspects of data protection including pseudonymization and anonymization procedures taking into account ethics committees requirements as well as the underlying legal framework are also presented. Without any exception, all principles and methods presented are best practices, repeatedly applied in different clinical environments and by no means theoretical considerations.
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Librería: Buchpark, Trebbin, AlemaniaBuchpark
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EUR 130,09
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Condición: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher | Establishing ethical and privacy protection aspects in scientific research, especially in medical research, has a long history. Medical data are usually more sensible than other personal data and require therefore an even higher degree of protectio…n than other personal data. In recent research projects genetic evaluations become more and more important and trigger thereby new and continuing activities in the context of data protection. Genetic data as a subset of medical data are the most sensible category of personal data and require therefore the highest degree of data protection. The book provides a systematic and itemized approach to data protection in clinical research including the handling of genetic material, genetic samples as well as derived genetic data and the subsequent secure storage of them. The set up of different kinds of clinical trials having in addition a genetic part, the concept of a genetic informed consent as well as collection schemes of samples are described in detail. Technical requirements and aspects of data protection including pseudonymization and anonymization procedures taking into account ethics committees requirements as well as the underlying legal framework are also presented. Without any exception, all principles and methods presented are best practices, repeatedly applied in different clinical environments and by no means theoretical considerations.
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Librería: AHA-BUCH GmbH, Einbeck, AlemaniaAHA-BUCH GmbH
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EUR 213,51
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Buch. Condición: Neu. Druck auf Anfrage Neuware - Printed after ordering - Establishing ethical and privacy protection aspects in scientific research, especially in medical research, has a long history. Medical data are usually more sensible than other personal data and require therefore an even higher degree of protection than…other personal data. In recent research projects genetic evaluations become more and more important and trigger thereby new and continuing activities in the context of data protection. Genetic data as a subset of medical data are the most sensible category of personal data and require therefore the highest degree of data protection.The book provides a systematic and itemized approach to data protection in clinical research including the handling of genetic material, genetic samples as well as derived genetic data and the subsequent secure storage of them. The set up of different kinds of clinical trials having in addition a genetic part, the concept of a genetic informed consent as well as collection schemes of samples are described in detail. Technical requirements and aspects of data protection including pseudonymization and anonymization procedures taking into account ethics committees requirements as well as the underlying legal framework are also presented.Without any exception, all principles and methods presented are best practices, repeatedly applied in different clinical environments and by no means theoretical considerations.
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Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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EUR 269,06
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Hardcover. Condición: Brand New. 1st edition. 198 pages. 9.53x6.85x0.63 inches. In Stock.
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Librería: Kennys Bookshop and Art Galleries Ltd., Galway, GY, IrlandaKennys Bookshop and Art Galleries Ltd.
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Condición: New. 2014. Hardcover. . . . . .
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Librería: Kennys Bookstore, Olney, MD, Estados Unidos de AmericaKennys Bookstore
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EUR 388,96
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Condición: New. 2014. Hardcover. . . . . . Books ship from the US and Ireland.
