Chapter 1 - History and Background of Oncology Clinical Trials
Chapter 1 examines the history and background of oncology clinical trials.
Edition:
3rd
Manual for Clinical Trials Nursing (Third Edition)
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The third edition of the Manual for Clinical Trials Nursing provides you with an updated examination of issues surrounding clinical trials.
Member Price: $99.00Nonmember Price: $129.60
ISBN:
978-1935864-370
Published By:
Oncology Nursing Society
Publication Date:
2015
Pages:
664
Chapters
Chapters 2 -3 - Drug Development, Types of Clinical Research: Background
Chapter 2 details drug development in clinical trials. CHapter 3 examines types of clinical research, focusing on background.
Chapters 4 -5 - Types of Clinical Research: Experimental, Types of Clinical Research: Observationals
Chapter 4 explores types of experimental clinical research and Chapter 5 examines types of observational clinical research.
Chapters 6 - 7 - Expanded Access to Investigational Drugs, Sponsoring Agencies
Chapter 6 explores issues surrounding the expandad access to investigational drugs. Chapter 7 examines sponsoring agencies.
Chapter 8 - Legal, Regulatory, and Legislative Issues
Chapter 8 delves into the legal, regulatory, and legislative issues surrounding clinical trials.
Chapter 9 - Good Clinical Practice
Chapter 9 examines issues surrounding the term "good clinical practice."
Chapter 10 - The Research Team
Chapter 10 examines the make-up of the research team in clinical trials.
Chapter 11 - Standard Operating Procedures
Chapter 11 explains issues surrounding standard operating procedures of clinical trials.
Chapter 12 - Ethics of Clinical Research
Chapter 12 explores the ethics of clinical research.
Chapters 13 - 14 - Elements of Protocol, Informed Consent
Chapter 13 details the elements of protocol while Chapter 14 examines informed consent.
Chapter 15 - Protocol Development and Response Assessment
Chapter 14 details protocol development and response assessment in clinical trials.
Chapter 16 - Protocol Review and Approval Process
Chapter 16 examines the protocol review and approval process in clinical trials.
Chapter 17 - Workload Determination and Resource Allocation
Chapter 17 details issues surrounding workload determination and resource allocation in clinical trials.
Chapter 18 - Billing, Budgets, and Funding
Chapter 18 examines issues surrounding billing, budgets, and funding in clinical trials.
Chapters 19 - 22 - Agreements and Contracts, Financial Risk Assessment and Monitoring, Internal Financial Audit and Quality Assurance, Financial Conflict of Interest
Chapter 19 outlines agreements and contracts. Chapter 20 examines risk assessment and monitoring. Chapter 21 details internal financial audit and quality assurance, while Chapter 22 examines financial conflict of interest.
Chapter 23 - Public and Patient Education
Chapter 23 describes issues surrounding public and patient education in clinical trials.
Chapter 24 - Accrual Base, Recruitment, and Promotion Strategies
Chapter 24 examines issues surrounding the accrual base, recruitment, and promotional strategies of clinical trials.
Chapters 25 - 26 - Adherence and Retention in Clinical Trials, Clinical Trial Registries
Chapter 25 details adherence and retention in clinical trials. Chapter 26 examines issues surrounding clinical trial registries.
Chapter 27 - Investigational Agents: Procurement, Accountability, and Administration of Research Study Drugs
Chapter 27 examines issues surrounding investigational agents, detailing procurement, accountability, and administration of research study drugs.
Chapter 28 - Adverse Events
Chapter 28 examines adverse events in clinical trials.
Chapter 29 - Patient and Family Education
Chapter 29 explores issues surrounding patient and family education of clinical trials.
Chapter 30 - Psychosocial Distress
Chapter 30 examines issues surrounding psychosocial distress.
Chapter 31 - Pharmacogenetics and Pharmacogenomics
Chapter 31 focuses on issues surrounding pharmacogenetics and pharmacogenomics.
Chapter 32 - Genetic Testing
Chapter 32 examines issues surrounding genetic testing.
Chapters 33 - 34 - Cytogenetics, Tumor Profiling
Chapter 33 examines issues surrounding cytogenetics. Chapter 34 explores tumor profiling.
Chapters 35 - 36 - Storage of Genetic Material, Pharmacokinetic Trials
Chapter 35 examines the storage of genetic material.
Chapters 37 - 38 - Documentation, Data Management and Electronic Data Management Systems
Chapter 37 examines documentation of clinicial trials. Chapter 38 explores issues surrounding data management and electronic data management systems.
Chapter 39 - Creating and Maintaining a Regulatory File
Chapter 39 examines how to create and maintain regulatory files.
Chapters 40 - 41 - Data and Safety Monitoring Plans, Preparing for Audits, Inspections, and Monitoring Visits
Chapter 40 details data and safety monitoring plans. Chapter 41 examines issues surrounding preparing for audits, inspections, and monitoring visits.
Chapters 42 - 43 - Clinical Trial Nurse Education, Mentorship
Chapter 42 details clinical trial nursing education. Chapter 43 examines mentorship.
Chapter 44 - Publishing Guidance for Clinical Trial Nurses
Chapter 44 provides publishing guidance for clinical trials nurses.
Chapter 45 - Australia
Chapter 45 examines clinical trials in Australia.
Chapter 46 - Austria
Chapter 46 details clinical trials in Austria.
Chapter 47 - Belarus
Chapter 47 examines clinical trials in Belarus.
Chapter 48 - Canada
Chapter 48 explains clinical trials in Canada.
Chapter 49 - China
Chapter 49 examines clinical trials in China.
Chapter 50 - European Union Directives
Chapter 50 examines clinical trials in European Union Directives.
Chapter 51 - France
Chapter 51 examines clinical trials in France.
Chapter 52 - Germany
Chapter 52 examines clinical trials in Germany.
Chapter 53 - India
Chapter 53 examines clinical trials in India.
Chapter 54 - Ireland
Chapter 54 details clinical trials in Ireland.
Chapter 55 - Italy
Chapter 55 details clinical trials in Italy.
Chapter 56 - Japan
Chapter 56 details clinical trials in Japan.
Chapter 57 - Mexico
Chapter 57 details clinical trials in Mexico.
Chapter 58 - New Zealand
Chapter 58 examines clinical trials in New Zealand.
Chapter 59 - Romania
Chapter 59 details clinical trials in Romania.
Chapter 60 - Spain
Chapter 60 details clinical trials in Spain.
Chapter 61 - Thailand
Chapter 61 details clinical trials in Thailand.
Chapter 62 - United Kingdom
Chapter 62 details clinical trials in the United Kingdom.
Appendices
Collects the book's appendices.