top

  Info

  • Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.

  Info

  • Utilizzare questo link per rimuovere la selezione effettuata.

Biblioteca

MARC Lista (tabellare)
Principles and practice of clinical research [[electronic resource] /] / [edited by] John I. Gallin, Frederick P. Ognibene
Principles and practice of clinical research [[electronic resource] /] / [edited by] John I. Gallin, Frederick P. Ognibene
Edizione [2nd ed.]
Pubbl/distr/stampa Amsterdam ; ; Boston, : Elsevier/Academic Press, c2007
Descrizione fisica 1 online resource (447 p.)
Disciplina 616.0072
Altri autori (Persone) GallinJohn I
OgnibeneFrederick P
Soggetto topico Clinical medicine - Research
Soggetto genere / forma Electronic books.
ISBN 1-281-05227-2
9786611052270
0-08-048956-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front cover; Principles and Practice of Clinical Research; Copyright page; Table of contents; Preface; Acknowledgements; Contributors; Chapter 1: A Historical Perspective on Clinical Research; 1. THE EARLIEST CLINICAL RESEARCH; 2. THE GREEK AND ROMAN INFLUENCE; 3. MIDDLE AGES AND RENAISSANCE; 4. SEVENTEENTH CENTURY; 5. EIGHTEENTH CENTURY; 6. NINETEENTH CENTURY; 7. TWENTIETH CENTURY AND BEYOND; Acknowledgment; References and Notes; PART I: ETHICAL, REGULATORY, AND LEGAL ISSUES; Chapter 2: Ethical Principles in Clinical Research; 1. DISTINGUISHING CLINICAL RESEARCHFROM CLINICAL PRACTICE
2. WHAT DOES ETHICS HAVE TO DOWITH CLINICAL RESEARCH?3. HISTORY OF ETHICAL ATTENTION TOCLINICAL RESEARCH; 4. CODES OF RESEARCH ETHICSAND REGULATIONS; 5. ETHICAL FRAMEWORK FORCLINICAL RESEARCH; 6. ETHICAL CONSIDERATIONS IN RANDOMIZED CLINICAL TRIALS; 7. CONCLUSION; References; Chapter 3: Researching a Bioethical Question; 1. TYPES OF BIOETHICAL ISSUES; 2. TYPES OF BIOETHICAL RESEARCH METHODOLOGIES; 3. EXAMPLES OF IMPORTANT BIOETHICAL RESEARCH; 4. SPECIAL CONSIDERATIONS INBIOETHICAL RESEARCH; References and Notes; Chapter 4: Integrity in Research: Individual and Institutional Responsibility
1. GUIDELINES FOR THE CONDUCTOF RESEARCH2. SCIENTIFIC INTEGRITY AND MISCONDUCT; 3. MENTOR-TRAINEE RELATIONSHIPS; 4. DATA ACQUISITION, MANAGEMENT, SHARING, AND OWNERSHIP; 5. RESEARCH INVOLVING HUMAN AND ANIMAL SUBJECTS; 6. COLLABORATIVE SCIENCE; 7. CONFLICT OF INTEREST AND COMMITMENT; 8. PEER REVIEW; 9. PUBLICATION PRACTICES AND RESPONSIBLE AUTHORSHIP; Acknowledgment; References; Chapter 5: Institutional Review Boards; 1. HISTORICAL, ETHICAL, ANDREGULATORY FOUNDATIONSOF CURRENT REQUIREMENTSFOR RESEARCH INVOLVINGHUMAN SUBJECTS; 2. INSTITUTIONAL REVIEW BOARDS; 3. CLINICAL RESEARCHERSAND IRBs
4. THE CURRENT IRB SYSTEM UNDER EVALUATION5. CONCLUSION; References and Notes; Chapter 6: Data and Safety Monitoring Boards; 1. DESCRIPTION OF THE DATA ANDSAFETY MONITORING BOARD; 2. DATA AND SAFETY MONITORINGBOARD FUNCTIONS; 3. DATA AND SAFETY MONITORINGBOARD DECISION MAKING; 4. EXAMPLES; 5. CONCLUSIONS; References; Chapter 7: Data Management in Clinical Trials; 1. THE RESEARCH TEAM; 2. PLANNING THE TRIAL; 3. WHERE ARE DATA?; 4. WHO CAN COLLECT DATA?; 5. SITE INITIATION VISIT; 6. INFORMED CONSENT; 7. ELIGIBILITY; 8. REGISTRATION; 9. WHAT DATA DO YOU COLLECT?; 10. TREATMENT PLAN
11. CONCURRENT THERAPY12. ADVERSE EVENT MONITORING; 13. ROUTINE MONITORING VISITS; 14. AUDIT TRAIL; 15. ELECTRONIC DATABASE; 16. SUMMARY; References; Chapter 8: Unanticipated Risk in Clinical Research; 1. THE REASONS; 2. THE DRUG; 3. THE TARGET; 4. THE TRIALS; 5. CASSANDRA REVEALED; 6. EXTENDED STUDIES; 7. FIAU TOXICITY; 8. REASSESSING THEPRECLINICAL STUDIES; 9. RESEARCH OVERSIGHT; 10. THE INVESTIGATIONS BEGIN; 11. SCIENTIFIC MISCONDUCT; 12. THE FDA; 13. THE NATIONAL INSTITUTES OF HEALTH; 14. THE INSTITUTE OF MEDICINE; 15. THE MEDIA; 16. THE CONGRESS; 17. THE LAW; 18. EPILOGUE
Acknowledgments
Record Nr. UNINA-9910458652203321
Amsterdam ; ; Boston, : Elsevier/Academic Press, c2007
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Principles and practice of clinical research [[electronic resource] /] / [edited by] John I. Gallin, Frederick P. Ognibene
Principles and practice of clinical research [[electronic resource] /] / [edited by] John I. Gallin, Frederick P. Ognibene
Edizione [2nd ed.]
Pubbl/distr/stampa Amsterdam ; ; Boston, : Elsevier/Academic Press, c2007
Descrizione fisica 1 online resource (447 p.)
Disciplina 616.0072
Altri autori (Persone) GallinJohn I
OgnibeneFrederick P
Soggetto topico Clinical medicine - Research
ISBN 1-281-05227-2
9786611052270
0-08-048956-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front cover; Principles and Practice of Clinical Research; Copyright page; Table of contents; Preface; Acknowledgements; Contributors; Chapter 1: A Historical Perspective on Clinical Research; 1. THE EARLIEST CLINICAL RESEARCH; 2. THE GREEK AND ROMAN INFLUENCE; 3. MIDDLE AGES AND RENAISSANCE; 4. SEVENTEENTH CENTURY; 5. EIGHTEENTH CENTURY; 6. NINETEENTH CENTURY; 7. TWENTIETH CENTURY AND BEYOND; Acknowledgment; References and Notes; PART I: ETHICAL, REGULATORY, AND LEGAL ISSUES; Chapter 2: Ethical Principles in Clinical Research; 1. DISTINGUISHING CLINICAL RESEARCHFROM CLINICAL PRACTICE
2. WHAT DOES ETHICS HAVE TO DOWITH CLINICAL RESEARCH?3. HISTORY OF ETHICAL ATTENTION TOCLINICAL RESEARCH; 4. CODES OF RESEARCH ETHICSAND REGULATIONS; 5. ETHICAL FRAMEWORK FORCLINICAL RESEARCH; 6. ETHICAL CONSIDERATIONS IN RANDOMIZED CLINICAL TRIALS; 7. CONCLUSION; References; Chapter 3: Researching a Bioethical Question; 1. TYPES OF BIOETHICAL ISSUES; 2. TYPES OF BIOETHICAL RESEARCH METHODOLOGIES; 3. EXAMPLES OF IMPORTANT BIOETHICAL RESEARCH; 4. SPECIAL CONSIDERATIONS INBIOETHICAL RESEARCH; References and Notes; Chapter 4: Integrity in Research: Individual and Institutional Responsibility
1. GUIDELINES FOR THE CONDUCTOF RESEARCH2. SCIENTIFIC INTEGRITY AND MISCONDUCT; 3. MENTOR-TRAINEE RELATIONSHIPS; 4. DATA ACQUISITION, MANAGEMENT, SHARING, AND OWNERSHIP; 5. RESEARCH INVOLVING HUMAN AND ANIMAL SUBJECTS; 6. COLLABORATIVE SCIENCE; 7. CONFLICT OF INTEREST AND COMMITMENT; 8. PEER REVIEW; 9. PUBLICATION PRACTICES AND RESPONSIBLE AUTHORSHIP; Acknowledgment; References; Chapter 5: Institutional Review Boards; 1. HISTORICAL, ETHICAL, ANDREGULATORY FOUNDATIONSOF CURRENT REQUIREMENTSFOR RESEARCH INVOLVINGHUMAN SUBJECTS; 2. INSTITUTIONAL REVIEW BOARDS; 3. CLINICAL RESEARCHERSAND IRBs
4. THE CURRENT IRB SYSTEM UNDER EVALUATION5. CONCLUSION; References and Notes; Chapter 6: Data and Safety Monitoring Boards; 1. DESCRIPTION OF THE DATA ANDSAFETY MONITORING BOARD; 2. DATA AND SAFETY MONITORINGBOARD FUNCTIONS; 3. DATA AND SAFETY MONITORINGBOARD DECISION MAKING; 4. EXAMPLES; 5. CONCLUSIONS; References; Chapter 7: Data Management in Clinical Trials; 1. THE RESEARCH TEAM; 2. PLANNING THE TRIAL; 3. WHERE ARE DATA?; 4. WHO CAN COLLECT DATA?; 5. SITE INITIATION VISIT; 6. INFORMED CONSENT; 7. ELIGIBILITY; 8. REGISTRATION; 9. WHAT DATA DO YOU COLLECT?; 10. TREATMENT PLAN
11. CONCURRENT THERAPY12. ADVERSE EVENT MONITORING; 13. ROUTINE MONITORING VISITS; 14. AUDIT TRAIL; 15. ELECTRONIC DATABASE; 16. SUMMARY; References; Chapter 8: Unanticipated Risk in Clinical Research; 1. THE REASONS; 2. THE DRUG; 3. THE TARGET; 4. THE TRIALS; 5. CASSANDRA REVEALED; 6. EXTENDED STUDIES; 7. FIAU TOXICITY; 8. REASSESSING THEPRECLINICAL STUDIES; 9. RESEARCH OVERSIGHT; 10. THE INVESTIGATIONS BEGIN; 11. SCIENTIFIC MISCONDUCT; 12. THE FDA; 13. THE NATIONAL INSTITUTES OF HEALTH; 14. THE INSTITUTE OF MEDICINE; 15. THE MEDIA; 16. THE CONGRESS; 17. THE LAW; 18. EPILOGUE
Acknowledgments
Record Nr. UNINA-9910784640603321
Amsterdam ; ; Boston, : Elsevier/Academic Press, c2007
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Principles and practice of clinical research [[electronic resource] /] / [edited by] John I. Gallin, Frederick P. Ognibene
Principles and practice of clinical research [[electronic resource] /] / [edited by] John I. Gallin, Frederick P. Ognibene
Edizione [2nd ed.]
Pubbl/distr/stampa Amsterdam ; ; Boston, : Elsevier/Academic Press, c2007
Descrizione fisica 1 online resource (447 p.)
Disciplina 616.0072
Altri autori (Persone) GallinJohn I
OgnibeneFrederick P
Soggetto topico Clinical medicine - Research
ISBN 1-281-05227-2
9786611052270
0-08-048956-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front cover; Principles and Practice of Clinical Research; Copyright page; Table of contents; Preface; Acknowledgements; Contributors; Chapter 1: A Historical Perspective on Clinical Research; 1. THE EARLIEST CLINICAL RESEARCH; 2. THE GREEK AND ROMAN INFLUENCE; 3. MIDDLE AGES AND RENAISSANCE; 4. SEVENTEENTH CENTURY; 5. EIGHTEENTH CENTURY; 6. NINETEENTH CENTURY; 7. TWENTIETH CENTURY AND BEYOND; Acknowledgment; References and Notes; PART I: ETHICAL, REGULATORY, AND LEGAL ISSUES; Chapter 2: Ethical Principles in Clinical Research; 1. DISTINGUISHING CLINICAL RESEARCHFROM CLINICAL PRACTICE
2. WHAT DOES ETHICS HAVE TO DOWITH CLINICAL RESEARCH?3. HISTORY OF ETHICAL ATTENTION TOCLINICAL RESEARCH; 4. CODES OF RESEARCH ETHICSAND REGULATIONS; 5. ETHICAL FRAMEWORK FORCLINICAL RESEARCH; 6. ETHICAL CONSIDERATIONS IN RANDOMIZED CLINICAL TRIALS; 7. CONCLUSION; References; Chapter 3: Researching a Bioethical Question; 1. TYPES OF BIOETHICAL ISSUES; 2. TYPES OF BIOETHICAL RESEARCH METHODOLOGIES; 3. EXAMPLES OF IMPORTANT BIOETHICAL RESEARCH; 4. SPECIAL CONSIDERATIONS INBIOETHICAL RESEARCH; References and Notes; Chapter 4: Integrity in Research: Individual and Institutional Responsibility
1. GUIDELINES FOR THE CONDUCTOF RESEARCH2. SCIENTIFIC INTEGRITY AND MISCONDUCT; 3. MENTOR-TRAINEE RELATIONSHIPS; 4. DATA ACQUISITION, MANAGEMENT, SHARING, AND OWNERSHIP; 5. RESEARCH INVOLVING HUMAN AND ANIMAL SUBJECTS; 6. COLLABORATIVE SCIENCE; 7. CONFLICT OF INTEREST AND COMMITMENT; 8. PEER REVIEW; 9. PUBLICATION PRACTICES AND RESPONSIBLE AUTHORSHIP; Acknowledgment; References; Chapter 5: Institutional Review Boards; 1. HISTORICAL, ETHICAL, ANDREGULATORY FOUNDATIONSOF CURRENT REQUIREMENTSFOR RESEARCH INVOLVINGHUMAN SUBJECTS; 2. INSTITUTIONAL REVIEW BOARDS; 3. CLINICAL RESEARCHERSAND IRBs
4. THE CURRENT IRB SYSTEM UNDER EVALUATION5. CONCLUSION; References and Notes; Chapter 6: Data and Safety Monitoring Boards; 1. DESCRIPTION OF THE DATA ANDSAFETY MONITORING BOARD; 2. DATA AND SAFETY MONITORINGBOARD FUNCTIONS; 3. DATA AND SAFETY MONITORINGBOARD DECISION MAKING; 4. EXAMPLES; 5. CONCLUSIONS; References; Chapter 7: Data Management in Clinical Trials; 1. THE RESEARCH TEAM; 2. PLANNING THE TRIAL; 3. WHERE ARE DATA?; 4. WHO CAN COLLECT DATA?; 5. SITE INITIATION VISIT; 6. INFORMED CONSENT; 7. ELIGIBILITY; 8. REGISTRATION; 9. WHAT DATA DO YOU COLLECT?; 10. TREATMENT PLAN
11. CONCURRENT THERAPY12. ADVERSE EVENT MONITORING; 13. ROUTINE MONITORING VISITS; 14. AUDIT TRAIL; 15. ELECTRONIC DATABASE; 16. SUMMARY; References; Chapter 8: Unanticipated Risk in Clinical Research; 1. THE REASONS; 2. THE DRUG; 3. THE TARGET; 4. THE TRIALS; 5. CASSANDRA REVEALED; 6. EXTENDED STUDIES; 7. FIAU TOXICITY; 8. REASSESSING THEPRECLINICAL STUDIES; 9. RESEARCH OVERSIGHT; 10. THE INVESTIGATIONS BEGIN; 11. SCIENTIFIC MISCONDUCT; 12. THE FDA; 13. THE NATIONAL INSTITUTES OF HEALTH; 14. THE INSTITUTE OF MEDICINE; 15. THE MEDIA; 16. THE CONGRESS; 17. THE LAW; 18. EPILOGUE
Acknowledgments
Record Nr. UNINA-9910822795903321
Amsterdam ; ; Boston, : Elsevier/Academic Press, c2007
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Quantile regression in clinical research : complete analysis for data at a loss of homogeneity / / Ton J. Cleophas, Aeilko H. Zwinderman
Quantile regression in clinical research : complete analysis for data at a loss of homogeneity / / Ton J. Cleophas, Aeilko H. Zwinderman
Autore Cleophas Ton J.
Pubbl/distr/stampa Cham, Switzerland : , : Springer, , [2022]
Descrizione fisica 1 online resource (283 pages)
Disciplina 610.727
Soggetto topico Clinical medicine - Research
Quantile regression
Medicina clínica
Soggetto genere / forma Llibres electrònics
ISBN 3-030-82840-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910520075303321
Cleophas Ton J.  
Cham, Switzerland : , : Springer, , [2022]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The Quintessence of Basic and Clinical Research and Scientific Publishing / / Gowraganahalli Jagadeesh, Pitchai Balakumar, and Fortunato Senatore, editors
The Quintessence of Basic and Clinical Research and Scientific Publishing / / Gowraganahalli Jagadeesh, Pitchai Balakumar, and Fortunato Senatore, editors
Edizione [First edition.]
Pubbl/distr/stampa Singapore : , : Springer, , [2023]
Descrizione fisica 1 online resource (926 pages)
Disciplina 616.0072
Soggetto topico Clinical medicine - Research
Medical publishing
ISBN 981-9912-84-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 1. The Roadmap to Research: Fundamentals of a Multifaceted Research Process -- Chapter 2. Processes involved in the generation of novel ideas -- Chapter 3. Creativity and critical thinking contribute to scholarly achievement -- Chapter 4. Writing protocols in Pharmacological studies -- Chapter 5. Basics of Designing General Toxicology Studies -- Chapter 6. General design considerations in Reproductive and developmental toxicity studies -- Chapter 7. Genetic toxicology studies -- Chapter 8. Rodent Carcinogenicity Studies.-Chapter 9. Designing studies in pharmaceutical and medicinal chemistry -- Chapter 10. Experimental protocols in phytochemistry and natural products: an ever-evolving challenge -- Chapter 11. Drug substance/ product quality analysis (Quality assessment) -- Chapter 12. Drug Delivery Systems: Lipid Nanoparticles Technology in Clinic -- Chapter 13. Pharmacokinetic studies for drug development -- Chapter 14. New Alternative Methods in drug safety assessment -- Chapter 15. Animal models for the study of human disease -- Chapter 16. Physiologically based Pharmacokinetic Modelling in Drug Discovery and Clinical Development: A Treatise on Concepts, Model Workflow, Credibility, Application and Regulatory Landscape -- Chapter 17. Design and conduct of pharmacokinetics studies influenced by extrinsic factors -- Chapter 18. Specific Populations: Clinical Pharmacology Considerations -- Chapter 19. Impact of genetic variation on drug response.-Chapter 20. Phases of clinical trials -- Chapter 21. Common clinical trial designs -- Chapter 22. Elements of clinical trial protocol design -- Chapter 23. Good clinical practice in clinical trials, substantial evidence of efficacy, and interpretation of the evidence -- chapter 24. Grandfathered Drugs of 1938 in the United States -- Chapter 25. General overview of the statistical issues in clinical study designs -- Chapter 26. Introduction to pharmacoepidemiology and its application in clinical research -- Chapter 27. Pharmacovigilance through phased clinical trials, post-marketing surveillance and ongoing life cycle safety -- Chapter 28. The design and statistical analysis of randomized pre-clinical experiments -- Chapter 29. Descriptive and Inferential Statistics in Biomedical Sciences: an overview -- Chapter 30. Principles and applications of statistics in biomedical research: parametric and non-parametric tests including tests employed for Post-hoc analysis -- Chapter 31. Artificial intelligence generative chemistry design of target-specific scaffold-focused small molecule drug libraries -- Chapter 32. Artificial intelligence technologies for clinical data pharmacoanalytics. Case studies on Alzheimer’s disease -- Chapter 33. Bioinformatics: Theory and Application -- Chapter 34. Drug targets and drug discovery research -- Chapter 35. Role of Nonclinical Programs in Drug Development -- Chapter 36. Drug repurposing: strategies and study design in bringing back old drugs to the mainline -- Chapter 37. Empowering knowledge on efficient literature search: an overview of biomedical search engines and databases -- Chapter 38. Literature Reviews: An Overview of Systematic, Integrated, and Scoping Review -- Chapter 39. How To Create A Bibliography -- Chapter 40. Publication metrics /Bibliometrics -- Chapter 41. How to write a scientific paper -- Chapter 42. Preparing and structuring a manuscript for publication -- Chapter 43. Writing a scientific article -- Chapter 44. How to Present Results in a Research Paper -- Chapter 45. Communicating results of quantitative research -- Chapter 46. How to Efficiently Write a Persuasive Discussion Section -- Chapter 47. Submitting a manuscript for publication, the peer review process, and getting past the gatekeepers -- Chapter 48. Writing a Postgraduate or Doctoral Thesis: A Step-by-Step Approach -- Chapter 49. Poster presentation at scientific meetings -- Chapter 50. Strategies for the preparation and delivery of oral presentation -- Chapter.-51. Grant Process and Peer Review ─ US National Institutes of Health System -- Chapter 52. Rigor and specifics in writing research proposal -- Chapter 53. Writing research grant proposals ─ from an Indian Perspective -- Chapter 54. Funding opportunities (resources) in biomedical sciences: Indian perspective -- Chapter 55. Mentorship in biomedical sciences -- chapter 56. Commercializing the technology – transitioning from the academic lab to the market -- Chapter 57. Patent law fundamentals for biomedical scientists -- Chapter 58. Research integrity: responsible conduct of research -- Chapter 59. Publication integrity, authorship, and misconduct.
Record Nr. UNINA-9910746973703321
Singapore : , : Springer, , [2023]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Research Partners with Lived Experience [[electronic resource] ] : Stories from Patients and Survivors / / edited by Andrew Stranieri, Grant Meredith, Selena Firmin
Research Partners with Lived Experience [[electronic resource] ] : Stories from Patients and Survivors / / edited by Andrew Stranieri, Grant Meredith, Selena Firmin
Autore Stranieri Andrew
Edizione [1st ed. 2024.]
Pubbl/distr/stampa Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2024
Descrizione fisica 1 online resource (196 pages)
Disciplina 353.6
Altri autori (Persone) MeredithGrant
FirminSelena
Soggetto topico Public health administration
Clinical medicine - Research
Biomedical engineering
Social medicine
Patient education
Health Administration
Clinical Research
Medical and Health Technologies
Health, Medicine and Society
Patient Education
ISBN 981-9700-33-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1 Paradigm shift: The lived experience of a researcher with postural orthostatic tachycardia syndrome -- 2 Who punched me in the back? Becoming a CKD researcher -- 3 Zebras have spots -- 4 To be, or not to be, that is the question: Stuttering into Academia -- 5 Living with Family Violence and The Great Escape -- 6 My journey: from patient to researcher with lived experience -- 7 A Duty of Care To Improve Processes.—8 Better Health through Integrative Medicine: A Pursuit of Lived Experience -- 9 My Personal, Professional, and Academic Journey and Lived Experience with Domestic Violence -- Endometriosis -- 11 A peek into the life of an Asthmatic -- 12 You have to be courageous -- 13 Living with Anxiety and Severe Depression -- 14 Its in your head! -- 15 How Lived Experience Mediated My Gold, Ribbons, Puzzles and Morals Research Motivations: a Reflective Introspection.
Record Nr. UNINA-9910847074003321
Stranieri Andrew  
Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2024
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The role of purchasers and payers in the clinical research enterprise [[electronic resource] ] : workshop summary / / Sean Tunis, Allan Korn, and Alex Ommaya, editors ; based on a workshop of the Clinical Research Roundtable, Board on Health Sciences Policy, Institute of Medicine
The role of purchasers and payers in the clinical research enterprise [[electronic resource] ] : workshop summary / / Sean Tunis, Allan Korn, and Alex Ommaya, editors ; based on a workshop of the Clinical Research Roundtable, Board on Health Sciences Policy, Institute of Medicine
Pubbl/distr/stampa Washington, D.C., : National Academy Press, c2002
Descrizione fisica 1 online resource (120 p.)
Altri autori (Persone) TunisSean
KornAllan
OmmayaAlex
Soggetto topico Clinical medicine - Research
Clinical medicine
Soggetto genere / forma Electronic books.
ISBN 1-280-20954-2
9786610209545
0-309-59418-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910455973703321
Washington, D.C., : National Academy Press, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The role of purchasers and payers in the clinical research enterprise [[electronic resource] ] : workshop summary / / Sean Tunis, Allan Korn, and Alex Ommaya, editors ; based on a workshop of the Clinical Research Roundtable, Board on Health Sciences Policy, Institute of Medicine
The role of purchasers and payers in the clinical research enterprise [[electronic resource] ] : workshop summary / / Sean Tunis, Allan Korn, and Alex Ommaya, editors ; based on a workshop of the Clinical Research Roundtable, Board on Health Sciences Policy, Institute of Medicine
Pubbl/distr/stampa Washington, D.C., : National Academy Press, c2002
Descrizione fisica 1 online resource (120 p.)
Altri autori (Persone) TunisSean
KornAllan
OmmayaAlex
Soggetto topico Clinical medicine - Research
Clinical medicine
ISBN 0-309-18290-5
1-280-20954-2
9786610209545
0-309-59418-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910780131203321
Washington, D.C., : National Academy Press, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The role of purchasers and payers in the clinical research enterprise [[electronic resource] ] : workshop summary / / Sean Tunis, Allan Korn, and Alex Ommaya, editors ; based on a workshop of the Clinical Research Roundtable, Board on Health Sciences Policy, Institute of Medicine
The role of purchasers and payers in the clinical research enterprise [[electronic resource] ] : workshop summary / / Sean Tunis, Allan Korn, and Alex Ommaya, editors ; based on a workshop of the Clinical Research Roundtable, Board on Health Sciences Policy, Institute of Medicine
Pubbl/distr/stampa Washington, D.C., : National Academy Press, c2002
Descrizione fisica 1 online resource (120 p.)
Altri autori (Persone) TunisSean
KornAllan
OmmayaAlex
Soggetto topico Clinical medicine - Research
Clinical medicine
ISBN 0-309-18290-5
1-280-20954-2
9786610209545
0-309-59418-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910811900203321
Washington, D.C., : National Academy Press, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Sex and gender in biomedicine [[electronic resource] ] : theories, methodologies, results / / Ineke Klinge and Claudia Wiesemann (eds.)
Sex and gender in biomedicine [[electronic resource] ] : theories, methodologies, results / / Ineke Klinge and Claudia Wiesemann (eds.)
Edizione [North American ed., 1st University of Akron Press.]
Pubbl/distr/stampa [Akron, Ohio], : University of Akron Press, 2011
Descrizione fisica 1 online resource (127 p.)
Disciplina 610.724
Altri autori (Persone) KlingeGesine Thea <1949->
WiesemannClaudia
Soggetto topico Sex factors in disease - Research
Clinical medicine - Research
Medicine - Research
Soggetto genere / forma Electronic books.
ISBN 1-283-15245-2
9786613152459
1-935603-68-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910634070103321
[Akron, Ohio], : University of Akron Press, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui