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ISBN : 9781405195157
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—Robert Harrington, Professor of Medicine, Director, Duke Clinical Research Institute, Durham, North Carolina, USA
The Duke Clinical Research Institute (DCRI) is one of the world's leading academic clinical research organizations; its mission is to develop and share knowledge that improves the care of patients around the world through innovative clinical research. This concise handbook provides a practical "nuts and bolts" approach to the process of conducting clinical trials, identifying methods and techniques that can be replicated at other institutions and Medical practices.
Designed for investigators, research coordinators, CRO personnel, students, and others who have a desire to learn about clinical trials, this manual begins with an overview of the historical framework of clinical research, and leads the reader through a discussion of safety concerns and resulting regulations. Topics include Good Clinical Practice, informed consent, management of subject safety and data, as well as monitoring and reporting adverse events.
Updated to reflect recent regulatory and clinical developments, the manual reviews the conduct of clinical trials research in an increasingly global context. This new edition has been further expanded to include:
- In-depth information on conducting clinical trials of medical devices and biologics
- The role and responsibilities of Institutional Review Boards, and
- Recent developments regarding subject privacy concerns and regulations.
Ethical documents such as the Belmont Report and the Declaration of Helsinki are reviewed in relation to all aspects of clinical research, with a discussion of how researchers should apply the principles outlined in these important documents. This graphically appealing and eminently readable manual also provides sample forms and worksheets to facilitate data management and regulatory record retention; these can be modified and adapted for use at investigative sites.
- Paperback: 424 pages
- Publisher: Wiley-Blackwell; 2 edition (February 8, 2010)
- Language: English
- ISBN-10: 1405195150
- ISBN-13: 978-1405195157
- Product Dimensions: 0.9 x 6.6 x 9.4 inches
- Shipping Weight: 2 pounds (View shipping rates and policies)
A Clinical Trials Manual From The Duke Clinical Research Institute: Lessons from a Horse Named Jim
Preface.
List of Abbreviations.
1 Lessons from a Horse Named Jim and Other Events in History Affecting the Regulation of Clinical Research.
2 The Process: Developing New Drugs, Biologics, and Devices.
The Drug Development Process.
Developing New Devices.
Postmarketing Surveillance of Drugs, Biologics, and Devices.
3 Good Clinical Practice and the Regulations.
Good Clinical Practice.
Responsibilities in the Code of Federal Regulations.
Where to Obtain Information and Guidance for the Regulations and GCP.
4 Informed Consent and the Regulations.
What Is Informed Consent?
Ethical Codes Regarding Informed Consent.
Regulatory Requirements for Informed Consent.
The Informed Consent Process.
5 Institutional Review Boards.
What is an Institutional Review Board?
IRB Activities.
Types of IRB Review.
Communication between IRBs and Investigators.
Communication between IRBs and Study Sponsors.
IRB Records and Reports.
Accreditation of IRBs.
Registration.
6 Adverse Events and Unanticipated Problems Involving Risks to Subjects or Others.
Why Collect Adverse Event Data?
Adverse Events.
Unanticipated Problems Involving Risks to Subjects or Others.
Investigator Responsibilities.
IRB Responsibilities.
Sponsor Responsibilities.
7 Monitoring, Audits, and Inspections.
Monitoring Plan.
On-Site Monitoring.
In-House Monitoring.
Audits and Inspections.
8 The Principal Investigator, the Clinical Research Coordinator, and the Study Site.
The Principal Investigator.
Staffing to Support Clinical Trials.
Space and Resource Needs.
The Local Institutional Review Board.
9 The Protocol.
Common Components of a Protocol.
Background and Rationale.
Study Organization.
Objectives/Endpoints.
Study Design.
Study Population.
Study Treatment Plan.
Safety Assessment, Management, and Reporting.
Replacement of Withdrawn, Dropped Out, and Lost to Follow-up Subjects.
Statistical Aspects.
Subject Data and Record Retention.
Monitoring.
10 Study Feasibility: Reviewing a Specific Protocol.
Reviewing a Specific Protocol.
Should We Do this Study at Our Site?
11 Study Activities.
Study Start-up Phase.
Study Maintenance Phase.
Study Completion and Close-Out Phase.
12 Study Documents/Essential Documents.
Documents at Study Start-Up.
Documents While the Study is in Progress.
Documents at Study Close-out.
Maintaining Your Site Study File.
13 Management of Study Drugs, Biologics, and Devices.
Study Drugs and Biologics.
Study Devices.
14 Managing Clinical Trial Data.
HIPAA, the Privacy Rule, and Clinical Trial Data.
Guidelines and Regulations Regarding Clinical Trial Data.
Study Site Responsibilities Regarding Clinical Trial Data.
Source Document Verification of Clinical Trial Data.
Release of Protected Medical Information.
Confidentiality of Clinical Trial Data.
Endpoint Adjudication.
15 Global Health and International Trials.
International Clinical Trials.
Ethnic and Racial Differences.
Ethical Issues and Cultural Sensitivities.
Why International Trials Are Important.
International Regulations.
Concerns.
Future Efforts.
Appendices.
Epilogue (Lisa G. Berdan).
Glossary.
Index.
The content is fine, but this is a textbook and the kindle version has no page numbers which make reading assignments by page numbers impossible. Amazon sent me back some gibberish (after my online complaint) as to why there were no page numbers. But knowing that some of the kindle books do have page numbers and the hard copy of the book has page numbers there is no excuse for this book to not have page numbers that correspond to the hard copy book.By Jonathan Q. Davis
I have all new staff members read this book. It is fantastic! It is easy to read and gives you a great overview of the research profession and how it evolved. Also has form samples.By Teresa Marq
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