SEARCH
 


TOPIC CATEGORIES

TOPICS BY JOB FUNCTION

REGIONS

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.

Advanced Good Clinical Practice: Practical Application and Implementation
June 1-2, 2015 | Boston, MA

Introduction to Clinical Research
June 1-2, 2015 | Boston, MA

Monitoring Clinical Drug Studies: Intermediate
June 2-3, 2015 | San Diego, CA

Clinical Project Management: Intermediate
June 2-3, 2015 | Boston, MA

Adverse Events: Managing and Reporting for Medical Devices
June 2-3, 2015 | San Francisco, CA

The CRA Manager Course
June 2-3, 2015 | Philadelphia, PA

Basics of Post-Marketing Pharmacovigilance and the Beginner PV Auditor
June 8-9, 2015 | San Francisco, CA

Medical Device Approval Process: Preparation and Processing of 510(k)s, IDEs, and PMAs
June 9-10, 2015 | Philadelphia, PA

Monitoring Clinical Drug Studies: Beginner
June 16-18, 2015 | Boston, MA

Comprehensive Monitoring for Medical Devices
June 16-18, 2015 | Boston, MA

Statistical Concepts for Non-Statisticians
June 22-23, 2015 | Boston, MA

Effectively Writing Clinical Trial Protocols
June 23-24, 2015 | Boston, MA

Drug Safety and Pharmacovigilance: Effective Drug Safety Reporting and Surveillance
June 23-24, 2015 | Philadelphia, PA

Auditing Techniques for Clinical Research Professionals
June 23-24, 2015 | Philadelphia, PA

Risk-Based Monitoring: Successful Planning and Implementation
June 23, 2015 | Philadelphia, PA

CRA & CRC Beginner: Program
June 23-25, 2015 | Philadelphia, PA

Clinical Project Management: Advanced
June 24-25, 2015 | Philadelphia, PA

Drug Approval Process: Preparation and Processing of INDs and NDAs
June 24-25, 2015 | Philadelphia, PA

Working with CROs: Building a Partnership for Project Success
June 24-25, 2015 | Philadelphia, PA

Preparing IND Submissions: How to Organize, Write, Submit, and Track Submissions
June 25-26, 2015 | Boston, MA

Medical Writing Fundamentals: How to Write Regulatory Documents
June 25-26, 2015 | Boston, MA

Clinical Project Management: Introduction to Practical Clinical Trial Planning for Project Managers
July 14-15, 2015 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After June 12, costs are $1,795.00.

Informed Consent Content & Process Requirements for Biobanking Studies
July 17, 2015 | Toronto, ON
Take advantage of our $800.00 price by registering early!
* After June 15, costs are $1,000.00.

Advanced Post-Marketing Pharmacovigilance Auditing
July 21-22, 2015 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After June 18, costs are $1,795.00.

Clinical Trials for Medical Devices: Design and Development
July 21-22, 2015 | Philadelphia, PA
Take advantage of our $1,595.00 price by registering early!
* After June 18, costs are $1,795.00.

Monitoring Clinical Drug Studies: Beginner
July 21-23, 2015 | Philadelphia, PA
Take advantage of our $1,695.00 price by registering early!
* After June 18, costs are $1,895.00.

Auditing Techniques for Clinical Research Professionals
July 22-23, 2015 | San Diego, CA
Take advantage of our $1,595.00 price by registering early!
* After June 18, costs are $1,795.00.

Comprehensive Monitoring for Medical Devices
July 28-30, 2015 | Philadelphia, PA
Take advantage of our $1,695.00 price by registering early!
* After June 25, costs are $1,895.00.