Clinical Research Publications, Regulatory Guides, Industry Reports and Job Aids


Barnett's reference manuals, industry compendiums and job aids are designed to provide updates on important new developments in the industry. Following is a complete listing of our products.

Good Clinical Practice: A Question & Answer Reference Guide 2024/2025
$139.00
Good Clinical Practice: A Question & Answer Reference Guide 2024/2025 (Electronic)
$129.00
Biologics Development: A Regulatory Overview (2021)
$195.00
Expediting Drug & Biologics Development: A Strategic Approach 2021
$195.00
The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial Aspects of Clinical Research
$169.95

Good Clinical Practice: A Question & Answer Reference Guide 2024/2025
$139.00
Good Clinical Practice: A Question & Answer Reference Guide 2024/2025 (Electronic)
$129.00
Good Clinical Practice: A Question & Answer Reference Guide 2020/2021 (Electronic)
$69.95
Good Clinical Practice: A Question & Answer Reference Guide 2020/2021
$79.95
The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial Aspects of Clinical Research
$169.95
The Clinical Research Finance Roadmap Companion Reference Guide: Tools, Templates and Resources (Electronic)
$119.95
CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)
$99.00
CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)
$99.00
CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)
$99.00
CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)
$99.00
CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)
$99.00
CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)
$99.00
CRA Training Series: Volume 1 - An Overview of Drug Development (2018)
$99.00
CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)
$599.00
Study Site Training Series (2018): Volume 6: Understanding, Evaluating, and Implementing Clinical Protocols
$99.00
Study Site Training Series (2018): Volume 5: Your Role in Reporting Adverse Experiences
$99.00
Study Site Training Series (2018): Volume 4: Sponsor Visits and Regulatory Audits: What You Need to Know
$99.00
Study Site Training Series (2018): Volume 3: IRBs/IECs and Informed Consent: Protecting the Rights of Human Subjects
$99.00
Study Site Training Series (2018): Volume 2: FDA Clinical Research Regulations and GCPs: The Essentials
$99.00
Study Site Training Series (2018): Volume 1: The Clinical Study Site Team: Roles and Responsibilities
$99.00
Study Site Training Series (2018): A 6-Volume Self-Instructional Training Series for Investigative Teams
$499.00
HIPAA and U.S. Clinical Trials: A Question & Answer Reference Guide 2014
$45.95
State by State Clinical Trial Requirements (Print)
$99.95
The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors
$45.00
State-by-State Clinical Trial Requirements Reference Guide 2012 (electronic)
$89.95

Good Clinical Practice: A Question & Answer Reference Guide 2024/2025
$139.00
Good Clinical Practice: A Question & Answer Reference Guide 2024/2025 (Electronic)
$129.00
Good Clinical Practice: A Question & Answer Reference Guide 2020/2021 (Electronic)
$69.95
Good Clinical Practice: A Question & Answer Reference Guide 2020/2021
$79.95
The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial Aspects of Clinical Research
$169.95
The Clinical Research Finance Roadmap Companion Reference Guide: Tools, Templates and Resources (Electronic)
$119.95
CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)
$99.00
CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)
$99.00
CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)
$99.00
CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)
$99.00
CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)
$99.00
CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)
$99.00
CRA Training Series: Volume 1 - An Overview of Drug Development (2018)
$99.00
CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)
$599.00
Study Site Training Series (2018): Volume 6: Understanding, Evaluating, and Implementing Clinical Protocols
$99.00
Study Site Training Series (2018): Volume 5: Your Role in Reporting Adverse Experiences
$99.00
Study Site Training Series (2018): Volume 4: Sponsor Visits and Regulatory Audits: What You Need to Know
$99.00
Study Site Training Series (2018): Volume 3: IRBs/IECs and Informed Consent: Protecting the Rights of Human Subjects
$99.00
Study Site Training Series (2018): Volume 2: FDA Clinical Research Regulations and GCPs: The Essentials
$99.00
Study Site Training Series (2018): Volume 1: The Clinical Study Site Team: Roles and Responsibilities
$99.00
Study Site Training Series (2018): A 6-Volume Self-Instructional Training Series for Investigative Teams
$499.00
State by State Clinical Trial Requirements (Print)
$99.95
The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors
$45.00
State-by-State Clinical Trial Requirements Reference Guide 2012 (electronic)
$89.95

Biologics Development: A Regulatory Overview (2021)
$195.00
CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)
$599.00
CRA Training Series: Volume 1 - An Overview of Drug Development (2018)
$99.00
CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)
$99.00
CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)
$99.00
CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)
$99.00
CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)
$99.00
CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)
$99.00
CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)
$99.00
Expediting Drug & Biologics Development: A Strategic Approach 2021
$195.00
Good Clinical Practice: A Question & Answer Reference Guide 2020/2021
$79.95
Good Clinical Practice: A Question & Answer Reference Guide 2020/2021 (Electronic)
$69.95
Good Clinical Practice: A Question & Answer Reference Guide 2024/2025
$139.00
Good Clinical Practice: A Question & Answer Reference Guide 2024/2025 (Electronic)
$129.00
HIPAA and U.S. Clinical Trials: A Question & Answer Reference Guide 2014
$45.95
Medical Device Development: Regulation and Law (2020)
$195.00
New Drug Development: A Regulatory Overview (8th Edition)
$145.00
PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2018/2019 (Electronic + Hard Copy)
$1,300.00
PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2018/2019 (Hard Copy)
$545.00
State by State Clinical Trial Requirements (Print)
$99.95
State-by-State Clinical Trial Requirements Reference Guide 2012 (electronic)
$89.95
Study Site Training Series (2018): A 6-Volume Self-Instructional Training Series for Investigative Teams
$499.00
Study Site Training Series (2018): Volume 1: The Clinical Study Site Team: Roles and Responsibilities
$99.00
Study Site Training Series (2018): Volume 2: FDA Clinical Research Regulations and GCPs: The Essentials
$99.00
Study Site Training Series (2018): Volume 3: IRBs/IECs and Informed Consent: Protecting the Rights of Human Subjects
$99.00
Study Site Training Series (2018): Volume 4: Sponsor Visits and Regulatory Audits: What You Need to Know
$99.00
Study Site Training Series (2018): Volume 5: Your Role in Reporting Adverse Experiences
$99.00
Study Site Training Series (2018): Volume 6: Understanding, Evaluating, and Implementing Clinical Protocols
$99.00
The Clinical Research Finance Roadmap Companion Reference Guide: Tools, Templates and Resources (Electronic)
$119.95
The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial Aspects of Clinical Research
$169.95
The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors
$45.00
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