Author

Beer, Tomasz M

Axmaker, Larry

Place of Publication

New York, NY

Publisher

DiaMedica Publishing

Publication Date

2012

Physical Description

xxvi, 166 p. : ill. ; 23 cm.

Subjects

Neoplasms - therapy

Clinical Trials as Topic

Decision Making

Antineoplastic Protocols

Therapies, Investigational

Biomedical Research

United States

ISBN

9780982321973

Language

English

Material Type

Book

Audience

Patient or Public

Location

Vancouver Library

Vancouver Cancer Info Ctr

Kelowna Cancer Info Ctr

Victoria Cancer Info Ctr

Abbotsford Cancer Info Ctr

Prince George Cancer Info Ctr

Call Number

QZ267 B415 2012

Copies

Editor

Araujo, Raphael L. C.

Riechelmann, Rachel P.

Place of Publication

Cham, Switzerland

Publisher

Springer

Publication Date

2018

Physical Description

xii, 348 p. : ill. (chiefly col.) ; 25 cm.

Series

Proquest Ebook Central

Subjects

Neoplasms

Biomedical Research

Biostatistics - methods

Clinical Trials as Topic

Evidence-Based Medicine

ISBN

9783319713236

9783319713243

Language

English

Material Type

Book

Ebook

Audience

Professional

Location

Internet

Kelowna Library

Call Number

QZ206 M592 2018

Website Notes

This Proquest title is licensed for ONE BC Cancer staff user at a time. If you are denied access while on a network computer, please try again later.

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Alternate Title

How to meet international quality standard in clinical research

Author

Cingi, Cemal

Muluk, Nuray Bayar

Place of Publication

Cham, Switzerland

Publisher

Springer

Publication Date

2016

Series

EBSCOhost eBook

Subjects

Clinical Trials as Topic

Biomedical Research

Ethics, Research

Data Accuracy

Total Quality Management - standards

Internationality

Practice Guideline

Abstract

Table of Contents:

Chapter 1: Clinical Trials: Historical Aspects and Importance and New Drug Developments -- Chapter 2: The Definition of GCP -- Chapter 3: The Principles of GCP -- Chapter 4: The Drug Development Process and Evolution of Regulations -- Chapter 5: Planning Clinical Research -- Chapter 6: Preparation of Ethics Committee (IRB) Proposal -- Chapter 7: Preparation of Informed Consent -- Chapter 8: Preparation of Findings Tables -- Chapter 9: Setting the Ideal Statistical Methods -- Chapter 10: The Duties of a Clinical Research Coordinator

-- Chapter 11: The Duties of Clinical Researchers -- Chapter 12: The Phases of Clinical Studies -- Chapter 13: Safety in Clinical Trials -- Chapter 14: Setting the Size -- Chapter 15: Setting the Ideal Method -- Chapter 16: Ethics of Clinical Research -- Chapter 17: Recruitment and Enrolment -- Chapter 18: Why We Need Clinical Consent and Other Documentation -- Chapter 19: Monitoring the Trial -- Chapter 20: Inspection -- Chapter 21: Ethics: Institutional Review Board/Independent Ethics Committee (IRB/IEC) -- Chapter 22: Responsibilities of the Investigator -- Chapter 23: Responsibilities of the Sponsor -- Chapter 24: Clinical Trial Protocols

ISBN

9783319443430

9783319443447

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

This EBSCO title is licensed for one BC Cancer staff user at a time only. Authentication via HealthBC sign in required. Use your BC Cancer staff username and ID when prompted.