Checkout 0
Publications, Job Aids and Tools

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