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Following is a complete listing of Barnett's upcoming courses.  Courses are held multiple times each year in a variety of cities across the United States.

Auditing Techniques for Clinical Research Professionals
April 22-23, 2014 | San Diego, CA

Clinical Project Management: Advanced
April 22-23, 2014 | San Diego, CA

Comprehensive CRC Training
April 23-24, 2014 | Philadelphia, PA

The Highly Effective CRA: Soft Skills for Taking Your Work to the Next Level
May 6-7, 2014 | Philadelphia, PA

CRA & CRC: Beginner Program
May 6-8, 2014 | San Diego, CA

Monitoring Clinical Drug Studies: Intermediate
May 6-7, 2014 | San Diego, CA

Clinical Project Management: Introduction to Pratical Clinical Trial Planning for Project Managers
May 6-7, 2014 | Boston, MA

Developing Clinical Study Budgets
May 13, 2014 | Philadelphia, PA

Good Clinical Pratice for the Laboratory Scientist
May 13, 2014 | Philadelphia, PA

Investigator-Initiated Trials (IITs) and the Role and Responsibilities of the Investigator
May 14, 2014 | Philadelphia, PA

Regulatory Intelligence 101
May 19, 2014 | Philadelphia, PA

Advanced Good Clinical Practice: Practical Application and Implementation
June 2-3, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 2, costs are $1,795.00.

Monitoring Clinical Drug Studies: Advanced
June 3-4, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 2, costs are $1,795.00.

Biosimilar Products: Understanding FDA Requirements
June 4-5, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 2, costs are $1,795.00.

Clinical Project Management: Intermediate
June 4-5, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 2, costs are $1,795.00.

Data Management in the Electronic Data Capture Arena: Regulatory Considerations and Practical Applications for eCDM
June 4-5, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 2, costs are $1,795.00.

Trial Master Files: Why They Are Important and How to Organize Them
June 5, 2014 | Boston, MA
Take advantage of our $800.00 price by registering early!
* After May 5, costs are $1,000.00.

Case Report Form Design, Strategy, and Standards
June 6, 2014 | Philadelphia, PA
Take advantage of our $800.00 price by registering early!
* After May 5, costs are $1,000.00.

Adverse Events: Managing and Reporting for Pharmaceuticals
June 10-11, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 9, costs are $1,795.00.

Clinical Trial Documentation: Electronic Health Records, Essential Documents, and the Use of Notes to File
June 10, 2014 | Boston, MA
Take advantage of our $800.00 price by registering early!
* After May 9, costs are $1,000.00.

Developing CRAs as Site Study Managers
June 10-11, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 9, costs are $1,795.00.

Comprehensive Monitoring for Medical Devices
June 10-12, 2014 | Boston, MA
Take advantage of our $1,695.00 price by registering early!
* After May 9, costs are $1,895.00.

Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) in Site Management
June 11-12, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 9, costs are $1,795.00.

Medical Device Approval Process: Preparation and Processing of 510(k)s, IDEs, and PMAs
June 11-12, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 9, costs are $1,795.00.

Working with CROs: Building a Partnership for Project Success
June 12-13, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 12, costs are $1,795.00.

Introduction to Clinical Data Management
June 12-13, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 12, costs are $1,795.00.

Adverse Events: Managing and Reporting for Medical Devices
June 17-18, 2014 | San Diego, CA
Take advantage of our $1,595.00 price by registering early!
* After May 16, costs are $1,795.00.

Monitoring Clinical Drug Studies: Beginner
June 17-19, 2014 | Boston, MA
Take advantage of our $1,695.00 price by registering early!
* After May 16, costs are $1,895.00.

The CRA Manager Course
June 18-19, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 16, costs are $1,795.00.

Query Creation and Processing: Assessing Data Discrepancies and the Communications for Corrections
June 20, 2014 | Philadelphia, PA
Take advantage of our $800.00 price by registering early!
* After May 16, costs are $1,000.00.

Informed Consent - Beyond the Basics
June 20, 2014 | Philadelphia, PA
Take advantage of our $800.00 price by registering early!
* After May 16, costs are $1,000.00.

Statistical Concepts for Non-Statisticians
June 23-24, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

Risk-Based Monitoring: Successful Planning and Implementation
June 24, 2014 | Philadelphia, PA
Take advantage of our $800.00 price by registering early!
* After May 23, costs are $1,000.00.

Effectively Writing Clinical Trial Protocols
June 24-25, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

Drug Safety and Pharmacovigilance: Effective Drug Safety Reporting and Surveillance
June 24-25, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

CRA & CRC: Beginner Program
June 25-27, 2014 | Philadelphia, PA
Take advantage of our $1,695.00 price by registering early!
* After May 23, costs are $1,895.00.

Auditing Techniques for Clinical Research Professionals
June 25-26, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

Monitoring Clinical Drug Studies: Intermediate
June 25-26, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

Clinical Project Management: Advanced
June 25-26, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

Drug Approval Process: Preparation and Processing of INDs and NDAs
June 25-26, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

Preparing IND Submissions: How to Organize, Write, Submit, and Track Submissions
June 26-27, 2014 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After May 23, costs are $1,795.00.

The Pharmacovigilance Audit: How to Prepare for an Inspection
June 26, 2014 | Philadelphia, PA
Take advantage of our $800.00 price by registering early!
* After May 23, costs are $1,000.00.

Monitoring Clinical Drug Studies: Beginner
July 22-24, 2014 | Philadelphia, PA
Take advantage of our $1,695.00 price by registering early!
* After June 20, costs are $1,895.00.

Clinical Trials for Medical Devices: Design & Development
July 23-24, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After June 20, costs are $1,795.00.

Auditing Techniques for Clinical Research Professionals
July 29-30, 2014 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After June 27, costs are $1,795.00.

Comprehensive Monitoring for Medical Devices
July 29-31, 2014 | Philadelphia, PA
Take advantage of our $1,695.00 price by registering early!
* After June 27, costs are $1,895.00.

Clinical Project Management: Introduction to Pratical Clinical Trial Planning for Project Managers
July 30-31, 2014 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After June 27, costs are $1,795.00.

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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.


GCP for Investigators
 

Barnett’s scenario-based eLearning course is designed with the busy Principal Investigator in mind.  Based on real-life scenarios encountered by investigative site teams, this highly focused 7-module GCP training is designed to ensure comprehensive understanding of the key components of GCP.

For more details on this scenario-based eGCP program for investigators please click here. 


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

Jan - July 2014 Edition

Winter CatalogDownload Today!  

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

BCP Cover

Download Today! 

 

 

 


 

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)