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Biologics Development: A Regulatory Overview (2021)
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Medical Device Development: Regulation and Law (2020)
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PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2018/2019 (Electronic +
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CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)
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CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)
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CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)
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CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)
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CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)
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CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)
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CRA Training Series: Volume 1 - An Overview of Drug Development (2018)
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CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)
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Study Site Training Series (2018): Volume 6: Understanding, Evaluating, and
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Study Site Training Series (2018): Volume 5: Your Role in Reporting Adverse
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Study Site Training Series (2018): Volume 4: Sponsor Visits and Regulatory
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Study Site Training Series (2018): Volume 3: IRBs/IECs and Informed Consent:
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Study Site Training Series (2018): Volume 2: FDA Clinical Research Regulations
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Study Site Training Series (2018): Volume 1: The Clinical Study Site Team: Roles
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Study Site Training Series (2018): A 6-Volume Self-Instructional Training Series
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Good Clinical Practice: A Question & Answer Reference Guide 2018 (Electronic)
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CFR/ICH GCP Reference Guide for Medical Devices 2018 - Team 10-Pack
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CFR/ICH GCP Reference Guide 2018 - Team 10-Pack
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Good Clinical Practice: A Question & Answer Reference Guide 2017 (Electronic)
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State by State Clinical Trial Requirements (Print)
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Good Clinical Practice: A Question & Answer Reference Guide 2020/2021
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PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2018/2019 (Electronic +
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PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2018/2019 (Hard Copy)
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Good Clinical Practice: A Question & Answer Reference Guide 2020/2021
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Biologics Development: A Regulatory Overview (2021)
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CFR/ICH GCP Reference Guide 2018 - Team 10-Pack
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CFR/ICH GCP Reference Guide for Medical Devices 2018 - Team 10-Pack
$179.50
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CFR/ICH GCP Reference Guide for Medical Devices 2019 - Team 10-Pack
$179.50
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CFR/ICH GCP Reference Guide for Medical Devices 2020 - Team 10-Pack
$179.50
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CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)
$599.00
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CRA Training Series: Volume 1 - An Overview of Drug Development (2018)
$99.00
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CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)
$99.00
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CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)
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CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)
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CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)
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CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)
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CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)
$99.00
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Expediting Drug & Biologics Development: A Strategic Approach 2021
$195.00
Purchase

Glossary Acronyms for Clinical Research Professionals - Team 10-Pack
$199.50
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Good Clinical Practice: A Question & Answer Reference Guide 2017 (Electronic)
$65.95
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Good Clinical Practice: A Question & Answer Reference Guide 2018 (Electronic)
$69.95
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Good Clinical Practice: A Question & Answer Reference Guide 2020/2021
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Good Clinical Practice: A Question & Answer Reference Guide 2020/2021
(Electronic)
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Purchase

HIPAA and U.S. Clinical Trials: A Question & Answer Reference Guide 2014
$45.95
Purchase

Medical Device Development: Regulation and Law (2020)
$195.00
Purchase

New Drug Development: A Regulatory Overview (8th Edition)
$145.00
Purchase

PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2018/2019 (Electronic +
Hard Copy)
$1,300.00
Purchase

PAREXEL Biopharmaceutical R&D Statistical Sourcebook 2018/2019 (Hard Copy)
$545.00
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State by State Clinical Trial Requirements (Print)
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State-by-State Clinical Trial Requirements Reference Guide 2012 (electronic)
$89.95
Purchase

Study Site Training Series (2018): A 6-Volume Self-Instructional Training Series
for Investigative Teams
$499.00
Purchase

Study Site Training Series (2018): Volume 1: The Clinical Study Site Team: Roles
and Responsibilities
$99.00
Purchase

Study Site Training Series (2018): Volume 2: FDA Clinical Research Regulations
and GCPs: The Essentials
$99.00
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Study Site Training Series (2018): Volume 3: IRBs/IECs and Informed Consent:
Protecting the Rights of Human Subjects
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Study Site Training Series (2018): Volume 4: Sponsor Visits and Regulatory
Audits: What You Need to Know
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Study Site Training Series (2018): Volume 5: Your Role in Reporting Adverse
Experiences
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Study Site Training Series (2018): Volume 6: Understanding, Evaluating, and
Implementing Clinical Protocols
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The Clinical Research Finance Roadmap Companion Reference Guide: Tools,
Templates and Resources (Electronic)
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The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial
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The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and
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