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May 24, 2013
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DVD Phase I Study Management
May 10, 2013
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DVD Risk-Based Monitoring: The Data Management Connection
April 24, 2013
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DVD Strategies for Managing Difficult Clinical Research Sites
April 23, 2013
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DVD Data Quality in Clinical Trials: Rationale and Impact
April 22, 2013
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DVD Introduction to Data Management
April 16, 2013
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DVD Corrective Action Plans: Essential Documentation
April 8, 2013
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DVD Risk-Based Site Monitoring
April 4, 2013
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DVD Sponsor Management of Investigator Non-Compliance
April 1, 2013
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DVD Drug Development and FDA Regulations
March 21, 2013
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DVD Monitoring Reports: 10 Rules of Effective Report Writing
March 18, 2013
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DVD RECIST 1.0 & 1.1: Overview/Data Challenges in Oncology CT
March 13, 2013
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DVD Biosimilar Products: An Introduction to Approval Pathways
February 28, 2013
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DVD The IND in a CTD/eCTD Format
February 27, 2013
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DVD Trial Master File (TMF) for Sponsors: Set-Up and Maintenance
February 25, 2013
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DVD Developing Clinical Study Budgets for Sponsors
February 21, 2013
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DVD Critical Decision Points in Design & Conduct of Patient Registries
February 14, 2013
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DVD Monitoring Oncology Clinical Trials
February 13, 2013
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DVD Investigator Initiated Trials: Roles and Responsibilities
February 4, 2013
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DVD Improving Readability of SOPs and Other Procedural Documents
January 30, 2013
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DVD Writing Clinical Study Protocols
January 28, 2013
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DVD Use of Notes to File in Clinical Trial Essential Documentation
January 18, 2013
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DVD Building Relationships with Clinical Research Sites
January 11, 2013
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DVD The GCPs of Essential Documents
December 12, 2012
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DVD Electronic Medical Records
November 30, 2012
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DVD CRC & PI Current Practice Update: Impact of the FDA BIMO Program
November 15, 2012
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DVD Collaborating with CROs
November 9, 2012
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DVD Auditing Sponsors & CROs: Deconstruction & Application FDA CPGM
October 24, 2012
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DVD To Rejuvenate the Study or Not
October 17, 2012
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DVD Strategies for Remote Monitoring
September 12, 2012
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DVD Updates in Informed Consent Guidance
September 7, 2012
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DVD Protocol Deviations: Documenting, Managing, and Reporting
September 5, 2012
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DVD Principal Investigator Oversight & Appropriate Delegation
August 31, 2012
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DVD Medical Device Development: U.S. and EU Differences
August 30, 2012
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DVD Managing Observational Studies
August 23, 2012
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DVD Case Report Form Design, Strategy, and Standards
August 23, 2012
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DVD Writing SOPs and Procedural Documents
August 22, 2012
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DVD Developing and Negotiating Research Site Study Budgets & Contracts
August 15, 2012
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DVD ABCs of Clinical Research for Clinical Admin
August 13, 2012
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DVD Real-World Monitoring: Tips for Success and Sanity
August 6, 2012
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DVD Pediatric Clinical Drug Development
July 25, 2012
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DVD The New European Pharmacovigilance Legislation
July 18, 2012
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DVD Implications of New FDA Guideline Risk-Based Monitoring
July 16, 2012
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DVD Subject Recruitment: Proactive Project Plans & Issues Management
July 13, 2012
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DVD Design Considerations for GCP Training Programs
May 2, 2012
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DVD Good Clinical Practice: Practical Application and Implementation
April 26, 2012
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DVD CRC Role/Responsibilities Training
April 24, 2012
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DVD Adverse Event Monitoring for CRAs
April 13, 2012
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DVD Adverse Events for Medical Devices
April 9, 2012
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DVD Quality Risk Management in Clinical Trials and Pharmacovigilance
April 3, 2012
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DVD Preparing Clinical Research Sites for FDA Inspections
April 2, 2012
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DVD Strategies for Protocol Operationalization and Adherence
March 29, 2012
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DVD Implementation of Procedural Documents
March 16, 2012
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DVD Tools for Trainers: Clinical Research Job-Aids and Checklists
March 13, 2012
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DVD Preparing for SOP Inspection: An Auditor's Perspective
March 9, 2012
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DVD Worldwide Orphan Drug Designation Applications and Requirements
March 6, 2012
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DVD Five Key Strategic Steps for Developing Global SOPs
March 1, 2012
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DVD SOP on SOPs and Procedural Document Templates
February 20, 2012
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DVD Procedural Document System: Organized Development
February 1, 2012
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DVD Investigator Selection Criteria & Strategies
January 31, 2012
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DVD Adequate Sponsor Monitoring Systems
January 13, 2012
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DVD FDA's Bioresearch Monitoring (BIMO) Program: New Guidance
December 7, 2011
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DVD Principal Investigator Training: Roles and Responsibilities
November 17, 2011
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DVD Final FDA Guidance: How to Complete the FDA Form 1572
November 16, 2011
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DVD Monitoring Plan Development
November 15, 2011
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DVD Informed Consent Content & Process Requirements
November 1, 2011
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DVD Electronic Source Documentation
October 28, 2011
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DVD Implications of New FDA Guideline Risk-Based
October 18, 2011
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DVD Principal Investigator Oversight
September 27, 2011
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DVD Writing and Updating the Investigator's Brochure
September 26, 2011
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DVD Drug Safety and Pharmacovigilance
September 8, 2011
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DVD Preparing for a Safety Inspection
May 24, 2011
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DVD Informed Consent Form Review and Compliance: Onsite Strategies
May 12, 2011
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DVD Changes and Challenges in Foreign Clinical Research
April 15, 2011
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DVD Quality Systems: A Controlled Approach to GCP Compliance
April 12, 2011
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DVD Key Components of a Successful Study Site Start-up
March 30, 2011
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DVD Site Management and the Art of Assertiveness
March 24, 2011
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DVD GCP Training for Investigators
March 21, 2011
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DVD HIPAA Team Training
March 18, 2011
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DVD Vendor Management for the Clinical Data Manager
March 11, 2011
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DVD Writing and Maintaining the EU CTA (Clinical Trial Authorization)
March 8, 2011
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DVD Writing and Maintaining the Canadian CTA
March 7, 2011
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DVD HIPAA//HITECH Requirement Changes and Enforcement
March 4, 2011
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DVD Clinical Research Site Quality Improvement Strategies
February 23, 2011
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DVD Regulatory Intelligence
February 17, 2011
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DVD FDA Meetings Drugs and Biologics
February 16, 2011
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DVD Final FDA Guidance for Supervisory Responsibilities
February 16, 2011
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DVD Regulatory 101 Navigating the Background, Laws & Regulations
February 15, 2011
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DVD Final AE Regulatory Guidance
February 2, 2011
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DVD FDA Drug Approval Process
February 1, 2011
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DVD FDA Guidance: IRB Continuing Review of Clinical Investigations
January 12, 2011
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DVD Subject Recruitment for Clinical Research Sites
December 15, 2010
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DVD How to Prepare and Submit a Bullet Proof 510(k) Submission
December 14, 2010
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DVD Pediatric Drug Development
December 6, 2010
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DVD FDA Proposed Rule 2010: Sponsor Requirements to Report Fraud
December 3, 2010
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DVD Risk-Based Decisions in Clinical Trial Site Management
December 3, 2010
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DVD Clinical Trials for Pharmaceuticals: Design and Development
November 29, 2010
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DVD Making Good Teams Better: Taking Your Cross-Functional Global Team
November 11, 2010
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DVD Presentation Skills Training for Clinical Research Professionals
November 9, 2010
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DVD CRA Site Performance Improvement Monitoring Model
October 29, 2010
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DVD Introduction to the FDA
October 25, 2010
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DVD Introduction to Combination Products
October 22, 2010
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DVD FDA's Human Subject Protection /Bioresearch Monitoring Initiative
September 30, 2010
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DVD Examining Revisions to the FDA/ORA Compliance Guidance Manual
September 29, 2010
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DVD ABC of Clinical Research for Clinical Administrative Support Staff
September 13, 2010
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DVD Root Cause Analysis
August 26, 2010
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DVD Auditing Clinical Research Studies
August 26, 2010
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DVD Good Clinical Practice: Practical Application and Implementation
August 24, 2010
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DVD Medical Device Tracking
August 18, 2010
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DVD Approaches to Address Challenges in Vendor Management
August 13, 2010
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DVD Medical Device Reporting
August 11, 2010
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DVD Adverse Event Monitoring for CRAs
August 6, 2010
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DVD Train-the-Trainer: Successful Web-Based Training Strategies
July 27, 2010
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DVD Source Documentation: What is Adequate & Accurate?
July 20, 2010
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DVD Meeting HIPAA & FDA Requirements for Case Histories
July 20, 2010
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DVD Introduction to Signal Detection and Data Mining
June 28, 2010
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DVD Study Feasibility: Eliminating Low and Late Enrollment
June 23, 2010
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DVD Monitoring Phase I Clinical Trials
June 3, 2010
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DVD Essential Documentation in Clinical Trials at Research Sites
June 1, 2010
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DVD GCP Training: Core Human Subject Protection Training
May 24, 2010
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DVD Fraud in Clinical Research: An Overview
May 12, 2010
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DVD Site Relationship Management
May 11, 2010
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DVD Clinical Trial Design for Medical Devices
May 5, 2010
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DVD Adverse Events for Medical Devices
May 4, 2010
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DVD Electronic Medical Records and Source Document Verification
April 19, 2010
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DVD Transitioning Pharma Professionals to Medical Device Professionals
April 5, 2010
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DVD Developing and Negotiating Research Site Clinical Study Budgets
March 29, 2010
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DVD Monitoring Informed Consent: The Process and Document
March 29, 2010
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DVD Managing CRAs to Improve Performance & Study Outcomes
March 26, 2010
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On-Demand GCP Refresher Training 

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
For details on our scenario-based practical GCP application on-demand course, click here.

Barnett 'Hands-On' In-Person and Web Seminar Workshop Series
Barnett "Hands-On" Workshops are designed to provide intensive, hands-on training in a highly targeted clinical research topic area in a very interactive and engaging learning environment. To view more details and available courses, click here.

BARNETT CATALOGThe Barnett Catalogue is your comprehensive guide to the myriad live, web, and custom training opportunities offered throughout the year. 

Jan -  Jul 2013 Edition

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Aug 2013 -  Jan 2014 Edition

2013 Fall Catalog

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NEW! Blended Curriculum Path for the CRA, CRC, and Project Manager

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DVD IconWEB SEMINAR ARCHIVE 

View Catalog of Offerings   
New Titles added every month!
Course Alumni Save 50% 

Live SeminarLIVE SEMINARS

Monitoring Clinical Drug Studies: Intermediate 

Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 

Web SeminarWEB SEMINARS

10-Week CRA & CRC Beginner Program  

Trial Master File (TMF) for Sponsors: Set-Up and Maintenance 

Use of Notes to File in Clinical Trial Essential Documentation 

10-Week Clinical Research Associate (CRA) On-Boarding Program  

PublicationsPUBLICATIONS

2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)