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Barnett International's Core Curriculum courses are provided to you either in-person at a state-of-the-art meeting venue or in the form of live, interactive Web-based training offered via WebEx. Barnett's Goal is to provide you with a unique combination of strategy development and practical, hands-on content and course materials to enable you to get the most out of your training experience.

Clinical Project Management: Introduction to Practical Clinical Trial Planning for Project Managers
October 4-5, 2016 | Boston, MA

Pharmacokinetics: A Comprehensive Overview of Principles and Applications
October 4-5, 2016 | Philadelphia, PA

Auditing Techniques for Clinical Research Professionals
October 11-12, 2016 | San Francisco, CA

Monitoring Clinical Drug Studies: Beginner
October 11-13, 2016 | Philadelphia, PA

The Highly Effective CRA: Soft Skills for Taking Your Work to the Next Level
October 11-12, 2016 | San Francisco, CA

Adverse Events: Managing and Reporting for Pharmaceuticals
October 13-14, 2016 | San Francisco, CA

Preparing IND Submissions: How to Organize, Write, Submit, and Track Submissions
October 13-14, 2016 | Philadelphia, PA

Statistical Concepts for Non-Statisticians
October 17-18, 2016 | Boston, MA

Comprehensive Monitoring for Medical Devices
October 25-27, 2016 | Philadelphia, PA

Adverse Events: Managing and Reporting for Pharmaceuticals
November 1-2, 2016 | Philadelphia, PA

Introduction to Clinical Research
November 1-2, 2016 | San Diego, CA

Becoming a Preferred Site: Quality and Documentation Tips for Compliance
November 2, 2016 | San Diego, CA

WORKSHOP: How to Write Effective Monitoring Reports and Communications
November 2, 2016 | San Diego, CA

Investigator-Initiated Trials (IITs) and the Role and Responsibilities of the Investigator
November 3, 2016 | San Diego, CA
Take advantage of our $800.00 price by registering early!
* After October 3, costs are $1,000.00.

WORKSHOP: Trial Master Files: Why They Are Important and How to Organize Them
November 3, 2016 | San Diego, CA
Take advantage of our $800.00 price by registering early!
* After October 3, costs are $1,000.00.

Monitoring Clinical Drug Studies: Advanced
November 8-9, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After October 7, costs are $1,795.00.

Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) in Site Management
November 8-9, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After October 7, costs are $1,795.00.

The CRA Manager Course
November 8-9, 2016 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After October 7, costs are $1,795.00.

Drug Development and FDA Regulations
November 10, 2016 | Boston, MA
Take advantage of our $800.00 price by registering early!
* After October 7, costs are $1,000.00.

Clinical Project Management: Advanced
November 15-16, 2016 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After October 14, costs are $1,795.00.

Basics of Post-Marketing Pharmacovigilance and the Beginner PV Auditor
November 16-17, 2016 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After October 14, costs are $1,795.00.

Medical Device Approval Process: Preparation and Processing of 510(k)s, IDEs, and PMAs
November 16-17, 2016 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After October 14, costs are $1,795.00.

Clinical Project Management: Intermediate
November 30 - December 1, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After October 31, costs are $1,795.00.

Auditing Techniques for Clinical Research Professionals
December 1-2, 2016 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After October 31, costs are $1,795.00.

Drug Safety and Pharmacovigilance: Effective Drug Safety Reporting and Surveillance
December 1-2, 2016 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After October 31, costs are $1,795.00.

Effective Recruitment Planning and Management for Sponsors and CROs
December 1, 2016 | San Francisco, CA
Take advantage of our $800.00 price by registering early!
* After October 31, costs are $1,000.00.

Informed Consent: Beyond the Basics
December 2, 2016 | San Francisco, CA
Take advantage of our $800.00 price by registering early!
* After October 31, costs are $1,000.00.

Advanced Good Clinical Practice: Practical Application and Implementation
December 5-6, 2016 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

Adverse Events: Managing and Reporting for Medical Devices
December 6-7, 2016 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

CRA & CRC: Beginner Program
December 6-8, 2016 | Philadelphia, PA
Take advantage of our $1,695.00 price by registering early!
* After November 4, costs are $1,895.00.

Developing CRAs as Site Study Managers
December 6-7, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

Medical Device GCP Overview
December 6-7, 2016 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

Monitoring Oncology Clinical Trials
December 6-7, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

Statistical Concepts for Non-Statisticians
December 6-7, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

The Highly Effective CRA: Soft Skills for Taking Your Work to the Next Level
December 6-7, 2016 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

Clinical Project Management: Introduction to Practical Clinical Trial Planning for Project Managers
December 7-8, 2016 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After November 4, costs are $1,795.00.

WORKSHOP: Case Report Form Design, Strategy, and Standards
December 7, 2016 | Philadelphia, PA
Take advantage of our $800.00 price by registering early!
* After November 4, costs are $1,000.00.

How to Write Great SOPs and Work Instructions
December 8, 2016 | Philadelphia, PA
Take advantage of our $800.00 price by registering early!
* After November 7, costs are $1,000.00.

WORKSHOP: How to Write Effective Monitoring Reports and Communications
December 8, 2016 | Boston, MA
Take advantage of our $800.00 price by registering early!
* After November 7, costs are $1,000.00.

Comprehensive Monitoring for Medical Devices
December 13-15, 2016 | San Francisco, CA
Take advantage of our $1,695.00 price by registering early!
* After November 11, costs are $1,895.00.

Medical Writing Fundamentals: How to Write Regulatory Documents
December 13, 2016 | San Francisco, CA
Take advantage of our $800.00 price by registering early!
* After November 11, costs are $1,000.00.

Monitoring Clinical Drug Studies: Beginner
December 13-15, 2016 | Boston, MA
Take advantage of our $1,695.00 price by registering early!
* After November 11, costs are $1,895.00.

Working with CROs: Building a Partnership for Project Success
December 13-14, 2016 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After November 11, costs are $1,795.00.

Effectively Writing Clinical Trial Protocols
December 14-15, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After November 11, costs are $1,795.00.

Strategic Clinical Research Operational Planning: Applied Techniques for Cost Estimation, Risk Management, and Quality Assurance
December 15-16, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After November 11, costs are $1,795.00.

Monitoring Clinical Drug Studies: Intermediate
December 19-20, 2016 | Boston, MA
Take advantage of our $1,595.00 price by registering early!
* After November 18, costs are $1,795.00.

Advanced Post-Marketing Pharmacovigilance Auditing
December 20-21, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After November 18, costs are $1,795.00.

Preparing IND Submissions: How to Organize, Write, Submit, and Track Submissions
December 20-21, 2016 | San Francisco, CA
Take advantage of our $1,595.00 price by registering early!
* After November 18, costs are $1,795.00.

Conducting Clinical Trials Under ICH GCP
January 24-25, 2017 | San Diego, CA
Take advantage of our $1,595.00 price by registering early!
* After December 23, costs are $1,795.00.

Developing Clinical Study Budgets
January 24, 2017 | San Diego, CA
Take advantage of our $800.00 price by registering early!
* After December 23, costs are $1,000.00.

Monitoring Clinical Drug Studies: Advanced
January 24-25, 2017 | San Diego, CA
Take advantage of our $1,595.00 price by registering early!
* After December 23, costs are $1,795.00.

Optimizing Protocol Design and Strategies to Achieve Efficient, Lower Cost Trial Execution
January 30-31, 2017 | San Diego, CA
Take advantage of our $1,595.00 price by registering early!
* After December 23, costs are $1,795.00.