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Intro; Foreword; Contents; Abbreviations; 1: Introduction; 1.1 Acknowledgements; 1.2 Permissions; References; 2: How Quality Can Improve Reproducibility; 2.1 The Unknown of Reproducibility; 2.1.1 Irreproducibility and Retractions; 2.1.2 The Economics of Poor Reproducibility; 2.1.3 Reasons and Solutions; 2.2 What Is Quality; 2.3 Quality for Research; 2.4 Research Integrity; References; 3: Principles, References and Standards; 3.1 Quality Basics; 3.2 Total Quality Management; 3.2.1 The Process Approach; 3.2.2 Principles; 3.2.3 PDCA Cycle; 3.2.4 The Requirements

3.3 Quality Certification and Accreditation3.4 Quality Standards for Certification in Scientific Research; 3.4.1 ISO 9000; 3.4.2 Good Laboratory Practice; 3.4.3 ISO/IEC 17025; 3.4.4 Other References; References; 4: Quality and Basic Biomedical Research; 4.1 What Is Basic Biomedical Research; 4.2 Conscious Management; 4.3 Quality Throughout the Research Project; 4.3.1 Management of Study Contents and Controls; 4.3.1.1 Initial Requirements; 4.3.1.2 Controls and Metrics; 4.3.1.3 Documentation; 4.3.1.4 Training; 4.3.1.5 Communication; 4.3.1.6 Procurement

4.3.2 Management of the Research Project4.3.2.1 Planning; 4.3.2.2 Executing and Measuring; 4.3.2.3 Exploiting; 4.3.2.4 The Importance of Planned Controls (Shannon Eaker ); 4.4 International References and Models; 4.4.1 WHO-TDR Handbook on Quality Practices in Basic Biomedical Research; 4.4.2 Joint Code of Practice for Research: JCoPR (UK); 4.4.3 Research Quality Association Handbook and Guidelines; 4.4.4 Other Examples; 4.5 Quality Management in Basic Biomedical Research; 4.5.1 Organisation; 4.5.1.1 Quality Policy and Objectives; 4.5.1.2 Organisational Chart and Job Description

4.5.2 Quality System4.5.2.1 Quality Assurance and Quality Control; 4.5.2.2 Research Reviews; 4.5.3 Personnel; 4.5.3.1 Responsibility; 4.5.3.2 Competence, Skills and Motivation; 4.5.4 Physical Resources; 4.5.4.1 Economics; 4.5.4.2 Facilities; 4.5.4.3 Equipment; 4.5.4.4 Products for the Research; 4.5.4.5 Computer Systems; 4.5.5 Validation; 4.5.5.1 Protocols and Assay Validation; 4.5.5.2 Result Validation; 4.5.6 Documentation; 4.5.6.1 Prescriptive Documents; 4.5.6.2 Descriptive Documents; 4.5.6.3 Study Report; 4.5.7 Storage and Archiving; 4.5.7.1 Data Archiving

4.5.7.2 Sample Storage4.5.8 Health and Safety; 4.5.9 Publishing Practices; 4.5.10 Ethics; 4.6 Examples of Application; 4.6.1 Managing Research Resources in a Large Institute: The San Raffaele Experience (Daniele Zacchetti ); 4.6.2 A QMS for a Life Sciences Research Laboratory and Its Related Management Software (the qPMO WP3 Team ); 4.6.3 GLP as a Reference for Non-regulated Research (the MoBiLab Team ); References; 5: Quality Tools for the Scientific Research; 5.1 Tools for Project and Process Quality; 5.2 7 Basic Tools of TQM; 5.2.1 Pareto Chart

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