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Auditoría médica y epidemiología [[recurso electronico] /] / Francisco Álvarez Heredia
Auditoría médica y epidemiología [[recurso electronico] /] / Francisco Álvarez Heredia
Autore Álvarez Heredia Francisco
Pubbl/distr/stampa Bogotá, : Ecoe Ediciones, 2009
Descrizione fisica 1 online resource (271 p.)
Disciplina 610
Collana Ciencias de la salud
Soggetto topico Auditoría médica
Atención médica
Epidemiología
Medical audit
Medical care
Epidemiology
ISBN 958-771-231-5
1-4619-2164-3
1-4492-7715-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione spa
Nota di contenuto AUDITORÍA MÉDICA Y EPIDEMIOLOGÍA; PÁGINA LEGAL; TABLA DE CONTENIDO; CAPÍTULO 1; CAPÍTULO 2; CAPÍTULO 3; CAPÍTULO 4; CAPÍTULO 5; CAPÍTULO 6; CAPÍTULO 7; CAPÍTULO 8; CAPÍTULO 9; CAPÍTULO 10; CAPÍTULO 11; CAPÍTULO 12; CAPÍTULO 13; CAPÍTULO 14; CAPÍTULO 15; CAPÍTULO 16; CAPÍTULO 17; CAPÍTULO 18; BIBLIOGRAFÍA
Record Nr. UNINA-9910676680703321
Álvarez Heredia Francisco  
Bogotá, : Ecoe Ediciones, 2009
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Clinical audit
Clinical audit
Pubbl/distr/stampa [UK], : Dove Press
Disciplina 362.102305
Soggetto topico Medical audit
Medical Audit
Medical Administration & Management
Soggetto genere / forma Periodical
Periodicals.
ISSN 1179-2760
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-996336260103316
[UK], : Dove Press
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Clinical audit
Clinical audit
Pubbl/distr/stampa [UK], : Dove Press
Disciplina 362.102305
Soggetto topico Medical audit
Medical Audit
Medical Administration & Management
Soins médicaux - Évaluation
Soggetto genere / forma Periodical
Periodicals.
ISSN 1179-2760
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910140342003321
[UK], : Dove Press
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Clinical governance [[electronic resource] ] : a guide to implementation for healthcare professionals / / Rob McSherry and Paddy Pearce ; with a contribution by John Tingle
Clinical governance [[electronic resource] ] : a guide to implementation for healthcare professionals / / Rob McSherry and Paddy Pearce ; with a contribution by John Tingle
Autore McSherry Robert
Edizione [3rd ed.]
Pubbl/distr/stampa Chichester, U.K. ; ; Ames, Iowa, : Wiley-Blackwell, 2011
Descrizione fisica 1 online resource (217 p.)
Disciplina 362.1068
Altri autori (Persone) PearcePaddy
TingleJohn
Soggetto topico Medical care - Quality control
Medical audit
Clinical competence
Soggetto genere / forma Electronic books.
ISBN 1-118-78658-0
1-118-27602-7
1-283-40236-X
9786613402363
1-118-27601-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction and background : clinical governance and the national health service / Rob McSherry and Paddy Pearce -- What is clinical governance? / Rob McSherry and Paddy Pearce -- A guide to clinical governance / Rob McSherry and Paddy Pearce -- Applying clinical governance in daily practice / Rob McSherry and Paddy Pearce -- Identifying and exploring the barriers to the implementation of clinical governance / Rob McSherry and Paddy Pearce -- Clinical governance and the law / John Tingle -- The impact of clinical governance in the national health service / Rob McSherry and Paddy Pearce -- Education and training for clinical governance / Rob McSherry and Paddy Pearce.
Record Nr. UNINA-9910461845303321
McSherry Robert  
Chichester, U.K. ; ; Ames, Iowa, : Wiley-Blackwell, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Clinical governance [[electronic resource] ] : a guide to implementation for healthcare professionals / / Rob McSherry and Paddy Pearce ; with a contribution by John Tingle
Clinical governance [[electronic resource] ] : a guide to implementation for healthcare professionals / / Rob McSherry and Paddy Pearce ; with a contribution by John Tingle
Autore McSherry Robert
Edizione [3rd ed.]
Pubbl/distr/stampa Chichester, U.K. ; ; Ames, Iowa, : Wiley-Blackwell, 2011
Descrizione fisica 1 online resource (217 p.)
Disciplina 362.1068
Altri autori (Persone) PearcePaddy
TingleJohn
Soggetto topico Medical care - Quality control
Medical audit
Clinical competence
ISBN 1-118-78658-0
1-118-27602-7
1-283-40236-X
9786613402363
1-118-27601-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction and background : clinical governance and the national health service / Rob McSherry and Paddy Pearce -- What is clinical governance? / Rob McSherry and Paddy Pearce -- A guide to clinical governance / Rob McSherry and Paddy Pearce -- Applying clinical governance in daily practice / Rob McSherry and Paddy Pearce -- Identifying and exploring the barriers to the implementation of clinical governance / Rob McSherry and Paddy Pearce -- Clinical governance and the law / John Tingle -- The impact of clinical governance in the national health service / Rob McSherry and Paddy Pearce -- Education and training for clinical governance / Rob McSherry and Paddy Pearce.
Record Nr. UNINA-9910789897303321
McSherry Robert  
Chichester, U.K. ; ; Ames, Iowa, : Wiley-Blackwell, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Clinical governance : a guide to implementation for healthcare professionals / / Rob McSherry and Paddy Pearce ; with a contribution by John Tingle
Clinical governance : a guide to implementation for healthcare professionals / / Rob McSherry and Paddy Pearce ; with a contribution by John Tingle
Autore McSherry Robert
Edizione [3rd ed.]
Pubbl/distr/stampa Chichester, U.K. ; ; Ames, Iowa, : Wiley-Blackwell, 2011
Descrizione fisica 1 online resource (217 p.)
Disciplina 362.1068
Altri autori (Persone) PearcePaddy
TingleJohn
Soggetto topico Medical care - Quality control
Medical audit
Clinical competence
ISBN 9786613402363
9781118786581
1118786580
9781118276020
1118276027
9781283402361
128340236X
9781118276013
1118276019
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction and background : clinical governance and the national health service / Rob McSherry and Paddy Pearce -- What is clinical governance? / Rob McSherry and Paddy Pearce -- A guide to clinical governance / Rob McSherry and Paddy Pearce -- Applying clinical governance in daily practice / Rob McSherry and Paddy Pearce -- Identifying and exploring the barriers to the implementation of clinical governance / Rob McSherry and Paddy Pearce -- Clinical governance and the law / John Tingle -- The impact of clinical governance in the national health service / Rob McSherry and Paddy Pearce -- Education and training for clinical governance / Rob McSherry and Paddy Pearce.
Record Nr. UNINA-9910969722503321
McSherry Robert  
Chichester, U.K. ; ; Ames, Iowa, : Wiley-Blackwell, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Clinical trials audit preparation [[electronic resource] ] : a guide for good clinical practice (GCP) inspections / / Vera Mihajlovic-Madzarevic
Clinical trials audit preparation [[electronic resource] ] : a guide for good clinical practice (GCP) inspections / / Vera Mihajlovic-Madzarevic
Autore Mihajlovic-Madzarevic Vera
Pubbl/distr/stampa Hoboken, N.J., : John Wiley, 2010
Descrizione fisica 1 online resource (270 p.)
Disciplina 615.5/80724
Soggetto topico Drugs - Testing - Auditing
Medical audit
ISBN 0-470-92088-2
1-283-02484-5
9786613024848
0-470-57275-2
0-470-57274-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CLINICAL TRIALSAUDIT PREPARATION; CONTENTS; PREFACE; INTRODUCTION; Background History on Clinical Research Standards; GLOSSARY; CHAPTER 1 GOOD CLINICAL PRACTICE AND THERAPEUTIC PRODUCT DEVELOPMENT; 1.1 Good Clinical Practice in Clinical Research; 1.1.1 Definition; 1.1.2 GCP Compliance; 1.1.3 GCP Objectives; 1.1.4 Principles of ICH GCP; Clinical Trial Conduct; Risk Assessment; Subject's Rights and Safety; Background Information; Clinical Trial Protocol; Ethics Review and Approval; Medical Care of Trial Subject; Qualifications of Clinical Trial Personnel; Informed Consent Process
Data ManagementPatient Confidentiality; Investigational Product Manufacturing, Handling, and Storage; Quality Assurance; 1.1.5 GCP Applicability; 1.2 Role of the Sponsor of a Clinical Investigation; 1.2.1 GCP: Responsibilities of a Sponsor of a Clinical Trial; 1.2.2 Essential Documents for the Clinical Trial; Retention of the Essential Documents for the Clinical Trial; Archiving of the Essential Documents for the Clinical Trial After Discontinuation of Development; Notification; Transfer of Data Ownership; Records Retention; 1.2.3 Investigator Selection; Investigator's Qualifications
Resources at the Investigator's SiteProtocol and Investigator's Brochure; Agreement with the Investigator/Institution; 1.2.4 Allocation of Responsibilities; 1.2.5 Compensation to Subjects and Investigators; Compensation to Subjects for Trial-Related Injuries; Other types of Compensation to Trial Subjects; 1.2.6 Financing; 1.2.7 Notification/Submission to Regulatory Authorities; 1.2.8 Confirmation of Review by IRB/IEC; 1.2.9 Information on Investigational Products; 1.2.10 Manufacturing, Packaging, Labelling, and Coding Investigational Products
Characterization, Manufacturing, and Labeling of the Investigational ProductStorage Conditions; Packaging of the Investigational Product; Coding and Decoding of the Investigational Product; Investigational Product Changes and Bioequivalence Studies; 1.2.11 Supplying and Handling Investigational Products; Supply; Investigational Product Records; 1.2.12 Record Access; Verification of Patient Consent to Record Access; 1.2.13 Safety Information; Safety Issues; Communication of Safety Issues; 1.2.14 Adverse Drug Reaction Reporting; Serious Unexpected Adverse Drug Reactions
SAE Reporting ComplianceSafety Updates and Periodic Reports; 1.2.15 Monitoring; Purposes; Selection and Qualifications of Monitors; Monitoring Strategies; Monitor's Responsibilities; Monitoring Procedures; Monitoring Report; 1.2.16 Audit; Selection and Qualifications of Auditors; Auditing Procedures; Site Selection Criteria for Inspection; Reporting of Findings; Audit Certificate; 1.2.17 Noncompliance; 1.2.18 Premature Termination or Suspension of a Trial; 1.2.19 Clinical Trial/Study Reports; 1.2.20 Multicenter Trials
1.3 Role of the Institutional Review Board/Independent Ethics Committee (IRB/IEC)
Record Nr. UNINA-9910140166103321
Mihajlovic-Madzarevic Vera  
Hoboken, N.J., : John Wiley, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Clinical trials audit preparation : a guide for good clinical practice (GCP) inspections / / Vera Mihajlovic-Madzarevic
Clinical trials audit preparation : a guide for good clinical practice (GCP) inspections / / Vera Mihajlovic-Madzarevic
Autore Mihajlovic-Madzarevic Vera
Edizione [1st ed.]
Pubbl/distr/stampa Hoboken, N.J., : John Wiley, 2010
Descrizione fisica 1 online resource (270 p.)
Disciplina 615.5/80724
Soggetto topico Drugs - Testing - Auditing
Medical audit
ISBN 9786613024848
9780470920886
0470920882
9781283024846
1283024845
9780470572757
0470572752
9780470572740
0470572744
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CLINICAL TRIALSAUDIT PREPARATION; CONTENTS; PREFACE; INTRODUCTION; Background History on Clinical Research Standards; GLOSSARY; CHAPTER 1 GOOD CLINICAL PRACTICE AND THERAPEUTIC PRODUCT DEVELOPMENT; 1.1 Good Clinical Practice in Clinical Research; 1.1.1 Definition; 1.1.2 GCP Compliance; 1.1.3 GCP Objectives; 1.1.4 Principles of ICH GCP; Clinical Trial Conduct; Risk Assessment; Subject's Rights and Safety; Background Information; Clinical Trial Protocol; Ethics Review and Approval; Medical Care of Trial Subject; Qualifications of Clinical Trial Personnel; Informed Consent Process
Data ManagementPatient Confidentiality; Investigational Product Manufacturing, Handling, and Storage; Quality Assurance; 1.1.5 GCP Applicability; 1.2 Role of the Sponsor of a Clinical Investigation; 1.2.1 GCP: Responsibilities of a Sponsor of a Clinical Trial; 1.2.2 Essential Documents for the Clinical Trial; Retention of the Essential Documents for the Clinical Trial; Archiving of the Essential Documents for the Clinical Trial After Discontinuation of Development; Notification; Transfer of Data Ownership; Records Retention; 1.2.3 Investigator Selection; Investigator's Qualifications
Resources at the Investigator's SiteProtocol and Investigator's Brochure; Agreement with the Investigator/Institution; 1.2.4 Allocation of Responsibilities; 1.2.5 Compensation to Subjects and Investigators; Compensation to Subjects for Trial-Related Injuries; Other types of Compensation to Trial Subjects; 1.2.6 Financing; 1.2.7 Notification/Submission to Regulatory Authorities; 1.2.8 Confirmation of Review by IRB/IEC; 1.2.9 Information on Investigational Products; 1.2.10 Manufacturing, Packaging, Labelling, and Coding Investigational Products
Characterization, Manufacturing, and Labeling of the Investigational ProductStorage Conditions; Packaging of the Investigational Product; Coding and Decoding of the Investigational Product; Investigational Product Changes and Bioequivalence Studies; 1.2.11 Supplying and Handling Investigational Products; Supply; Investigational Product Records; 1.2.12 Record Access; Verification of Patient Consent to Record Access; 1.2.13 Safety Information; Safety Issues; Communication of Safety Issues; 1.2.14 Adverse Drug Reaction Reporting; Serious Unexpected Adverse Drug Reactions
SAE Reporting ComplianceSafety Updates and Periodic Reports; 1.2.15 Monitoring; Purposes; Selection and Qualifications of Monitors; Monitoring Strategies; Monitor's Responsibilities; Monitoring Procedures; Monitoring Report; 1.2.16 Audit; Selection and Qualifications of Auditors; Auditing Procedures; Site Selection Criteria for Inspection; Reporting of Findings; Audit Certificate; 1.2.17 Noncompliance; 1.2.18 Premature Termination or Suspension of a Trial; 1.2.19 Clinical Trial/Study Reports; 1.2.20 Multicenter Trials
1.3 Role of the Institutional Review Board/Independent Ethics Committee (IRB/IEC)
Record Nr. UNINA-9910813044303321
Mihajlovic-Madzarevic Vera  
Hoboken, N.J., : John Wiley, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Early warning system scores : a systematic review / / M. E. Beth Smith [and seven others]
Early warning system scores : a systematic review / / M. E. Beth Smith [and seven others]
Autore Smith M. E. Beth
Pubbl/distr/stampa Washington, District of Columbia : , : Department of Veterans Affairs (US), , [2014]
Descrizione fisica 1 online resource (iii, 39 pages) : illustrations
Disciplina 362.1
Collana Evidence-based synthesis program
Soggetto topico Medical care - Evaluation
Medical audit
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Early warning system scores
Record Nr. UNINA-9910717368903321
Smith M. E. Beth  
Washington, District of Columbia : , : Department of Veterans Affairs (US), , [2014]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Electronic health records [[electronic resource] ] : an audit and internal control guide / / Rebecca S. Busch
Electronic health records [[electronic resource] ] : an audit and internal control guide / / Rebecca S. Busch
Autore Busch Rebecca S
Edizione [1st edition]
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2008
Descrizione fisica 1 online resource (256 p.)
Disciplina 651.5/04261
Soggetto topico Medical records - Data processing
Medical audit
Electronic records - Access control
ISBN 0-470-39948-1
1-281-74423-9
9786611744236
0-470-39946-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Market background -- Industry applications -- Impact of e-health on case management -- Data in an e-health environment -- Algorithms -- Data-driven health decisions in an e-health environment -- Analytic tools and audit checklists -- Electronic health records -- Healthcare portfolio -- Conclusions.
Record Nr. UNINA-9910144137603321
Busch Rebecca S  
Hoboken, N.J., : Wiley, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
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