Skip to content

Insights Contact

Checkout 0

Total items in cart: 0 0

Training Solutions
Home
Explore Our Catalog
Insights
Contact

Home

Training Solutions

Training Courses
Training Portal Subscription

On-Site Training

Training Strategy Consulting

Publications

Explore Our Catalog

Account

Other sign in options Sign in

Orders
Profile

Account

Other sign in options Sign in

Orders
Profile

EXPLORE OUR CATALOG ▼

Products

Skip to results list

Availability

In stock
Out of stock

Price

$

to

$

The highest price is $2,195.00

Clear

365 items

Sort

Sort Alphabetically, A-Z

Featured Best selling Alphabetically, A-Z Alphabetically, Z-A Price, low to high Price, high to low Date, old to new Date, new to old

Filter

Availability

In stock
Out of stock

Price

$

to

$

The highest price is $2,195.00

Sort

Sort Alphabetically, A-Z

Featured Best selling Alphabetically, A-Z Alphabetically, Z-A Price, low to high Price, high to low Date, old to new Date, new to old

Stay Connected With Us

#Barnett

customer.service@barnettinternational.com

Phone: 1.215.413.2471

Toll-free within the US: 1.800.856.2556

Footer menu 1

About Us
Who We Serve
Contact
Accreditation, Policies, and Procedures

Footer menu 2

FAQs
Privacy Policy

Search

Products

10-Hour Advanced Clinical Project Management Skills Development

10-Hour Advanced Clinical Project Management Skills Development

$1,795.00
10-Hour Clinical Research Manager Skills Development Series

10-Hour Clinical Research Manager Skills Development Series

$1,795.00
10-Hour Clinical Trial Start-Up Series

10-Hour Clinical Trial Start-Up Series

$1,795.00
10-Week Advanced FDA Post-Marketing Pharmacovigilance Auditing

10-Week Advanced FDA Post-Marketing Pharmacovigilance Auditing

$2,195.00

Products

Archive: Procedural Document System: Organized Development

Archive: Protocol Deviations: Documenting, Managing, and Reporting

Archive: Quality by Design in Clinical Research: Is This Only for the Protocol?

Archive: Quality by Design: A Lean Six Sigma Approach to Risk-Based Mon.

Archive: Quality Risk Management in Clinical Trials and Pharmacovigilance

Archive: Quality Systems: A Controlled Approach to GCP Compliance

Archive: Re-Engineering the RFP and Bid Defense Meeting

Archive: Real-World Monitoring: Tips for Success and Sanity

Archive: Recent Trends in Noncompliance: Critical Review and Analysis of Recent Regulatory Letters and Communications from the FDA, EMA, and Health Canada

Archive: RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials

Archive: Regulatory Intelligence

Archive: Risk-Based Auditing: Effective Compliance Strategies

Archive: Risk-Based Monitoring and Quality Management of Clinical Trials: Recent Guidance Updates from the FDA and EMA

Archive: Risk-Based Monitoring for Sites: Prepare Your Site for Success

Archive: Risk-Based Monitoring: The Data Management Connection

Archive: Risk-Based Site Monitoring

Archive: Risk-Based Thinking: How Monitors Can Develop an Auditor's Perspective

Archive: Root Cause Analysis: Applying the Concept for Better Study Compliance Management

Archive: SDTM and CDASH: What's the Connection?

Archive: Site Management and the Art of Assertiveness

Archive: Social Media in Clinical Research

Archive: SOP on SOPs and Procedural Document Templates

Archive: Source Documentation: What is Adequate and Accurate?

Archive: Sponsor Management of Investigator Non-Compliance