February 8, 2010

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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.

2009 Code of Federal Regulations Reference Guide for Medical Devices

$13.95

Medical Device Development: Regulation and Law, All New Edition!

$195.00

PRD09E - PAREXEL's R&D Statistical Sourcebook 2009/2010 (eStats)

$1,200.00

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2009/2010 (Hardcopy)

$425.00

Good Clinical Practice: A Question & Answer Reference Guide 2009

$45.95

2009 CFR/ICH GCP Reference Guide (Perfect Bound)

$11.95

2009 CFR/ICH GCP Reference Guide (Spiral Bound)

$13.95

IND Submissions: A Primer

$295.00

The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors

$45.00

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2008/2009 (Hardcopy)

$425.00

The US Drug Approval Trends and Yearbook 2008/2009

$295.00

eStats: PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2008/2009 Elec. Access

$1,200.00

PAREXEL's Bio/Pharmaceutical R&D Statistical Sourcebook 2007/2008 (Hardcopy Only)

$425.00

Glossary Acronyms for Clinical Research Professionals

$19.95

eStats: PAREXEL's Bio/Pharmaceutical R&D Statistical Sourcebook 2007/2008 Electronic Access

$1,200.00

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

$145.00

Good Clinical Practice: A Question and Answer Reference Guide 2008

$45.95

2008 CFR/ICH GCP Reference Guide (Spiral Bound)

$13.95

2008 CFR/ICH GCP Reference Guide (Perfect Bound)

$11.95

State-by-State Clinical Trial Requirements Reference Guide 2006

$49.95

Good Clinical Practice: A Question & Answer Reference Guide 2007

$39.95

Biologics Development: A Regulatory Overview (2004)

$145.00

Expediting Drug and Biologics Development: A Strategic Approach 2006

$145.00

New Drug Development: A Regulatory Overview (7th Edition)

$145.00

The Global GCP Compliance Report 2006: US, EU, and Japan

$95.00

Part 11 and Drug Development: A Q&A Reference Guide (March, 2004)

$24.95

HIPAA and Human Subjects Research: A Question & Answer Reference Guide (March 2003)

$24.95

Medical Device Development: A Regulatory Overview (2000)

$145.00

New Drug Approval in the European Union (2002)

$195.00

New Drug Approval in Japan (2002)

$195.00

3-Volume Worldwide Pharmaceutical Regulation Series (2002)

$500.00

PAREXEL's Bio/Pharmaceutical R&D Statistical Sourcebook 2006 (Hardcopy Only)

$295.00

PAREXEL's Pharmaceutical R&D Statistical Sourcebook 2005/2006

$295.00

PAREXEL's Pharmaceutical R&D Statistical Sourcebook 2004/2005

$295.00

PAREXEL's Pharmaceutical R&D Statistical Sourcebook 2003/2004

$295.00

Good Clinical Practice: A Question and Answer Reference Guide 2006

$39.95

Good Clinical Practice: A Question and Answer Reference Guide 2005

$39.95

Good Clinical Practice: A Question and Answer Reference Guide 2004

$39.95

Good Clinical Practice: A Question and Answer Reference Guide 2003

$39.95

1 Year - U.S. Regulatory Reporter Newsletter for Addresses in North America

$395.00

1 Year - U.S. Regulatory Reporter Newsletter for Addresses in Europe

$425.00

1 Year - U.S. Regulatory Reporter Newsletter for International Addresses Outside of Europe

$445.00

2 Year - U.S. Regulatory Reporter Newsletter for Addresses in North America

$790.00

2 Year - U.S. Regulatory Reporter Newsletter for Addresses in Europe

$850.00

2 Year - U.S. Regulatory Reporter Newsletter for International Addresses Outside of Europe

$890.00

Study Site Curriculum Training Series (6 Volume Set) (1999)

$405.00

Study Site Series Vol. 1 - The Clinical Study Site Team (1999)

$79.00

Study Site Series Vol. 2 - FDA, Clinical Research Regulations and GCPs (1999)

$79.00

Study Site Series Vol. 3 - IRBs/IECs and Informed Consent (1999)

$79.00

Study Site Series Vol. 4 - Sponsor Visits and Regulatory Audits (1999)

$79.00

Study Site Series Vol. 5 - Your Role in Reporting Adverse Experiences (1999)

$79.00

Study Site Series Vol. 6 - Understanding, Evaluating and Implementing Clinical Protocols (1999)

$79.00

CRA Training Series (7 Volume Set) (2000)

$405.00

CRA Training Series Vol. 1 - An Overview of Drug Development (2000)

$79.00

CRA Training Series Vol. 2 - Identifying and Screening Investigators (2000)

$79.00

CRA Training Series Vol. 3 - Conducting the Pre-Study Visit (2000)

$79.00

CRA Training Series Vol. 4 - Conducting the Study Initiation Visits (2000)

$79.00

CRA Training Series Vol. 5 - Conducting Routine Monitoring Visits (2000)

$79.00

CRA Training Series Vol. 6 - The CRA's Reference for Adverse Events (2000)

$79.00

CRA Training Series Vol. 7 - Test Your Knowledge (2000)

$100.00

Global Biotechnology Product Registration (1997)

$245.00

New Drug Approval in Germany (1995)

$75.00

New Drug Approval in Italy (1995)

$75.00

New Drug Approval in the United Kingdom (1995)

$75.00

New Drug Approval in Spain (1997)

$75.00

New Drug Approval in Brazil (1995)

$75.00

New Drug Approval in South Korea (1995)

$75.00

New Drug Approval in Canada (1998)

$75.00

New Drug Approval in France (1996)

$75.00

Meeting GMP & ISO 9001 Expectations for Product Development (1996)

$145.00

Patient Appointment Reminder Cards

$12.95

Research Study Patient Label

$12.95

Research Study File Label

$12.95

Study Day Estimator Wheel

$9.95

Barnett News

Barnett Releases Medical Device Development: Regulation and Law

September 15, 2009

2009-2010 Statistical Sourcebook Data Presented at DIA

June 23, 2009

Barnett Announces it's First-Ever Clinical Trainer's Forum

April 15, 2009

Barnett releases new regulatory resource: IND: A Primer

March 2, 2009

Oncology drugs top new clinical trials in 2007

July 1, 2008

Barnett is Acquired by Cambridge Healthtech Institute

March 24, 2008