Checkout
Menu
Accreditation, Policies and Procedures
FAQs
Instructor Biographies
Hotel Information
Categories

Buy One Web Seminar Archive, Get One Free during the month of December! Use Promo Code BOGO19 at Checkout. Or contact Barnett Customer Service: +1 782.972.5400 or toll-free in the U.S. at 800.856.2556.


Web Seminar Archives are available in either USB Flash Drive or DVD Format.
Archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.


Archive: Ensuring Success Through Smarter Site Selection and Study Feasibility
November 26, 2019
ORDER NOW
Archive: Implementing Quality Agreements
November 22, 2019
ORDER NOW
Archive: FDA's Bioresearch Monitoring (BIMO) Program: Inspection of Sponsors, CROs, and Monitors
November 21, 2019
ORDER NOW
Archive: Auditing Sponsors and CROs: Deconstruction and Application of the FDA's Compliance Program Guidance Manual
November 19, 2019
ORDER NOW
Archive: Introduction to Statistics for Non-Statisticians
November 18, 2019
ORDER NOW
Archive: Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
November 18, 2019
ORDER NOW
Archive: The GCPs of Essential Documents
November 7, 2019
ORDER NOW
Archive: Informed Consent Procedure: Lessons Learned from Inspection Findings
November 4, 2019
ORDER NOW
Archive: Introduction to Clinical Research
October 29, 2019
ORDER NOW
Archive: Protocol Deviations: Documenting, Managing, and Reporting
October 28, 2019
ORDER NOW
Archive: Risk-Based Thinking: How Monitors Can Develop an Auditor's Perspective
October 21, 2019
ORDER NOW
Archive: Electronic Source Data in Clinical Investigations: Navigating the Final FDA Guidance
October 21, 2019
ORDER NOW
Archive: A Systematic Approach to Study Start-Up: Improving Site Activation
October 18, 2019
ORDER NOW
Archive: Introduction to Data Management
October 16, 2019
ORDER NOW
Archive: State Laws Governing Clinical Trial Regulatory Compliance
September 25, 2019
ORDER NOW
Archive: RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials
September 24, 2019
ORDER NOW
Archive: TMF/eTMF Audit Strategies
September 20, 2019
ORDER NOW
Archive: Use of Electronic Health Record Data in Clinical Investigations
September 18, 2019
ORDER NOW
Archive: Developing Clinical Study Budgets for Sponsors
September 17, 2019
ORDER NOW
Archive: Final ICH GCP E6 R2: Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsors-Investigators and Institutions)
September 17, 2019
ORDER NOW
Archive: ABCs of Clinical Research for Clinical Administrative Support Staff
September 3, 2019
ORDER NOW
Archive: Working with Clinical Research Sites: Strategic Planning and Operations for Sponsors and CROs
August 28, 2019
ORDER NOW
Archive: Building Quality by Design (QbD) and Risk-Based Quality Management (RBQM) Systems into Clinical Operations
August 12, 2019
ORDER NOW
Archive: Managing Phase I Clinical Trials
August 12, 2019
ORDER NOW
Archive: Monitoring Oncology Clinical Trials
August 1, 2019
ORDER NOW
Archive: Recent Trends in Noncompliance: Critical Review and Analysis of Recent Regulatory Letters and Communications from the FDA, EMA, and Health Canada
July 17, 2019
ORDER NOW
Archive: Writing Clinical Study Protocols
July 17, 2019
ORDER NOW
Archive: Drug Development and FDA Regulations
July 16, 2019
ORDER NOW
Archive: TMF/eTMF Regulatory Agency Expectations, Inspections, and Findings
June 21, 2019
ORDER NOW
Archive: eTMF Quality Oversight: A Risk-Based Approach
June 21, 2019
ORDER NOW
Archive: Establishing Quality Tolerance Limits
June 18, 2019
ORDER NOW
Archive: Final ICH GCP E6 R2 Addendum: Overview of Changes Impacting Sponsors, CROs, Clinical Investigators/Sites
June 13, 2019
ORDER NOW
Archive: Preparing Clinical Research Sites for FDA Inspections
June 12, 2019
ORDER NOW
Archive: Risk-Based Site Monitoring
June 11, 2019
ORDER NOW
Archive: The Revised HHS Common Rule: What You Need to Know Now
June 10, 2019
ORDER NOW
Archive: FDA Drug Approval Process
June 3, 2019
ORDER NOW
Archive: Trial Master File (TMF) for Sponsors: Set-Up and Maintenance
May 31, 2019
ORDER NOW
Archive: Developing and Negotiating Research Site Clinical Study Budgets and Contracts
May 30, 2019
ORDER NOW
Archive: Risk-Based Monitoring: The Data Management Connection
May 29, 2019
ORDER NOW
Archive: Clinical Trial Start-Up: Using a Work Breakdown Structure (WBS) for Effective Planning
May 23, 2019
ORDER NOW
Archive: Leading Teams in a Changing Clinical Research Environment
May 22, 2019
ORDER NOW
Archive: Regulatory Intelligence
May 22, 2019
ORDER NOW
Archive: ABCs of GCP and the 13 Principles of ICH GCP E6
May 10, 2019
ORDER NOW
Archive: Root Cause Analysis: Applying the Concept for Better Study Compliance Management
May 9, 2019
ORDER NOW
Archive: Corrective Action Plans: Essential Documentation of a Site's Response to GCP Deficiencies
May 2, 2019
ORDER NOW
Archive: Current FDA and EMA Inspection Findings: Lessons Learned
May 2, 2019
ORDER NOW
Archive: CAP and CLIA Requirements for Clinical Research Laboratories
May 1, 2019
ORDER NOW
Archive: Monitoring Visit Reports for Medical Device Studies
April 30, 2019
ORDER NOW
Archive: Monitoring Medical Device Trials: An Introduction
April 29, 2019
ORDER NOW
Archive: Case Report Form Design, Strategy, and Standards
April 24, 2019
ORDER NOW
Archive: Final ICH GCP E6 R2: Implementing Risk Management Approaches for Compliance
April 22, 2019
ORDER NOW
Archive: Data Quality in Clinical Trials: Rationale and Impact
April 17, 2019
ORDER NOW
Archive: Good Clinical Practice: Practical Application and Implementation
April 11, 2019
ORDER NOW
Archive: ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank
April 10, 2019
ORDER NOW
Archive: Medical Writing Fundamentals: How to Write Regulatory Documents
April 10, 2019
ORDER NOW
Archive: Investigator Initiated Trials: Roles and Responsibilities
April 9, 2019
ORDER NOW
Archive: Strategies for Having Difficult Conversations
March 26, 2019
ORDER NOW
Archive: Final ICH GCP E6 R2: Sponsor Quality Management - Risk-Based/Risk Management Requirements and Approaches for Compliance
March 21, 2019
ORDER NOW
Archive: Building Relationships with Clinical Research Sites
March 20, 2019
ORDER NOW
Archive: Principal Investigator Oversight and the Appropriate Delegation of Tasks
March 19, 2019
ORDER NOW
Archive: Monitoring Reports: 10 Rules of Effective Report Writing
March 18, 2019
ORDER NOW
Archive: Monitoring Plan Development
February 21, 2019
ORDER NOW
Archive: Coaching Skills for Leaders
February 7, 2019
ORDER NOW
Archive: Cases in Advanced GCP: A Problem-Solving Practicum
February 7, 2019
ORDER NOW
Archive: Final ICH GCP E6 R2: Impact on Clinical Data Management
January 30, 2019
ORDER NOW
Archive: Writing the Clinical Study Report
January 23, 2019
ORDER NOW
Archive: Adverse Event Monitoring for CRAs
January 16, 2019
ORDER NOW
Archive: The CRA Role in Risk-Based Monitoring: Strategies for Effective Remote Monitoring
December 17, 2018
ORDER NOW
Archive: Implications of the FDA Guidance for a Risk-Based Approach to Monitoring and EMA Reflection Paper Risk-Based Quality Management in Clinical Trials
December 14, 2018
ORDER NOW
Archive: Use of Notes to File in Clinical Trial Essential Documentation
November 13, 2018
ORDER NOW
Archive: Strategies for Managing Difficult Clinical Research Sites
September 6, 2018
ORDER NOW
Archive: Subject Recruitment: Proactive Project Plans and Issues Management
July 20, 2018
ORDER NOW
Archive: Source Documentation: What is Adequate and Accurate?
June 25, 2018
ORDER NOW
Archive: Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155
June 25, 2018
ORDER NOW
Archive: Managing CRAs to Improve Performance and Study Outcomes
June 21, 2018
ORDER NOW
Archive: EMA and MHRA Inspections: Successful Planning and Execution Tips and Techniques
June 12, 2018
ORDER NOW
Archive: Preparation, Management, and Response to Inspections and Audits
June 5, 2018
ORDER NOW
Archive: Electronic Medical Records: Approaches for Ensuring Source Document and 21 CFR Part 11 Required Components
May 17, 2018
ORDER NOW
Archive: Data Management Plan Creation: Content and Rationale
May 9, 2018
ORDER NOW
Archive: Writing and Updating the Investigator's Brochure
May 9, 2018
ORDER NOW
Archive: Final ICH GCP E6 R2: Changes Impacting Sponsors/CROs
May 8, 2018
ORDER NOW
Archive: FDA Medical Device Approval Process
May 7, 2018
ORDER NOW
Archive: Tools for Trainers: Clinical Research Job-Aids and Checklists
May 2, 2018
ORDER NOW
Archive: CRA Current Practice Update: Impact of the FDA Bioresearch Monitoring (BIMO) Program
April 26, 2018
ORDER NOW
Archive: The IND in a CTD/eCTD Format
April 25, 2018
ORDER NOW
Archive: HIPAA Team Training: Fundamental Training Specifically Clinical Research Settings
April 23, 2018
ORDER NOW
Archive: Approaches to Address Challenges in Vendor Management
March 15, 2018
ORDER NOW
Archive: Adequate Sponsor Monitoring Systems In Anticipation of FDA Sponsor GCP Inspections
January 30, 2018
ORDER NOW
Archive: CRO Partnership Management
November 22, 2017
ORDER NOW
Archive: Writing and Maintaining the EU Clinical Trial Authorization
November 8, 2017
ORDER NOW
Archive: Recent Trends in Noncompliance: Critical Review and Analysis
November 1, 2017
ORDER NOW
Archive: Managing Risks in Outsourced Clinical Trials
August 22, 2017
ORDER NOW
Archive: eTMF Implementation Strategies
June 2, 2017
ORDER NOW
Archive: Data Management in the Electronic Data Capture Arena
April 11, 2017
ORDER NOW
Archive: Case Narrative Writing for Reporting Adverse Events
March 23, 2017
ORDER NOW
Archive: Final AE Regulatory Guidance
March 13, 2017
ORDER NOW
Archive: Centralized TMF Management: The CRO Sponsor Partnership
March 10, 2017
ORDER NOW
Archive: Essential Documentation in Clinical Trials at Research Sites
March 2, 2017
ORDER NOW
Archive: Quality by Design in Clinical Research: Is This Only for the Protocol?
December 7, 2016
ORDER NOW
Archive: Fraud in Clinical Research: An Overview
November 9, 2016
ORDER NOW
Archive: Risk-Based Auditing: Effective Compliance Strategies
October 31, 2016
ORDER NOW
Archive: EMA and FDA Inspections: Key Differences and Similarities
October 25, 2016
ORDER NOW
Archive: Final FDA Guidance: How to Complete the Form FDA 1572
October 3, 2016
ORDER NOW
Archive: CRO Selection Criteria, Eval, & Establishing the Relationship
September 16, 2016
ORDER NOW
Archive: Establishing a Risk Management Framework for Clin Trial Conduct
August 24, 2016
ORDER NOW
Archive: Investigational Product Accountability Best Practices
July 20, 2016
ORDER NOW
Archive: Detecting Risk Signals in Protocols, Data, and Monitoring
July 19, 2016
ORDER NOW
Archive: Quality Systems: A Controlled Approach to GCP Compliance
May 19, 2016
ORDER NOW
Archive: Re-Engineering the RFP and Bid Defense Meeting
May 4, 2016
ORDER NOW
Archive: Annual GCP Training Update: MHRA Inspection Findings for 2015
February 29, 2016
ORDER NOW
Archive: Subject Enrollment: Creating Effective Enrollment Models
February 8, 2016
ORDER NOW
Archive: Principal Investigator/Site GCP Compliance and Performance
February 3, 2016
ORDER NOW
Archive: Data Management: Key Regulations Impacting the Role of the CDM
January 12, 2016
ORDER NOW
Archive: SDTM and CDASH: What's the Connection?
January 12, 2016
ORDER NOW
Archive: Quality Risk Management in Clinical Trials and Pharmacovigilance
December 10, 2015
ORDER NOW
Archive: Study Feasibility: Eliminating Low and Late Enrollment
November 24, 2015
ORDER NOW
Archive: Sponsor Management of Investigator Non-Compliance
November 20, 2015
ORDER NOW
Archive: Establishing a Vendor Management Program
November 16, 2015
ORDER NOW
Archive: Clinical Trials and the Sunshine Act
November 3, 2015
ORDER NOW
Archive: Sponsor Responsibilities for Global Drug Studies
October 5, 2015
ORDER NOW
Archive: Critical Decision Points in Design and Conduct of Patient Reg.
September 17, 2015
ORDER NOW
Archive: Strategies for Developing Effective Training & Facilitation Skills
July 23, 2015
ORDER NOW
Archive: Strategies for Ensuring Good Documentation Practices (GDP)
June 25, 2015
ORDER NOW
Archive: Principal Investigator Training: Roles and Responsibilities
May 18, 2015
ORDER NOW
Archive: Improving Readability of SOPs and Other Procedural Documents
May 5, 2015
ORDER NOW
Archive: Writing Protocols for Diagnostic Studies
April 15, 2015
ORDER NOW
Archive: Strategies for Conducting Vendor Audits
April 3, 2015
ORDER NOW
Archive: Quality by Design: A Lean Six Sigma Approach to Risk-Based Mon.
March 24, 2015
ORDER NOW
Archive: Study Initiation Strategies for Sponsors: Study and Site Start-Up
March 13, 2015
ORDER NOW
Archive: Risk-Based Monitoring for Sites: Prepare Your Site for Success
December 1, 2014
ORDER NOW
Archive: Using Data to Identify Risk Indicators in Risk-Based Monitoring
August 29, 2014
ORDER NOW
Archive: Social Media in Clinical Research
August 22, 2014
ORDER NOW
Archive: Auditor Emotional Intelligence
June 11, 2014
ORDER NOW
Archive: Monitoring Phase I Clinical Trials
May 23, 2014
ORDER NOW
Archive: Study Site Start-Up: Organization and Management Tips
May 6, 2014
ORDER NOW
Archive: Phase I Study Management
April 11, 2014
ORDER NOW
Archive: Writing Quality SOPs:Guidelines, Tools, Templates for SOP Creation
March 21, 2014
ORDER NOW
Archive: Strategies for Protocol Operationalization and Adherence
March 17, 2014
ORDER NOW
Archive: Real-World Monitoring: Tips for Success and Sanity
January 16, 2014
ORDER NOW
Archive: Preparing for SOP Inspection: An Auditor's Perspective
December 5, 2013
ORDER NOW
Archive: Trial Master File (TMF) for Research Sites: Set-Up and Maintenance
October 25, 2013
ORDER NOW
Archive: Writing Clinical Study Reports for Diagnostic Studies
October 17, 2013
ORDER NOW
Archive: GCP Training for Investigators
June 20, 2013
ORDER NOW
Archive: Informed Consent Content & Process Requirements
June 10, 2013
ORDER NOW
Archive: Managing Observational Studies
August 23, 2012
ORDER NOW
Archive: Writing SOPs and Procedural Documents
August 22, 2012
ORDER NOW
Archive: Design Considerations for GCP Training Programs
May 2, 2012
ORDER NOW
Archive: CRC Role/Responsibilities Training
April 24, 2012
ORDER NOW
Archive: Implementation of Procedural Documents
March 16, 2012
ORDER NOW
Archive: Five Key Strategic Steps for Developing Global SOPs
March 1, 2012
ORDER NOW
Archive: SOP on SOPs and Procedural Document Templates
February 20, 2012
ORDER NOW
Archive: Procedural Document System: Organized Development
February 1, 2012
ORDER NOW
Archive: Investigator Selection Criteria & Strategies
January 31, 2012
ORDER NOW
Archive: Site Management and the Art of Assertiveness
March 24, 2011
ORDER NOW
Archive: Making Good Teams Better: Taking Your Cross-Functional Global Team
November 11, 2010
ORDER NOW
Archive: Presentation Skills Training for Clinical Research Professionals
November 9, 2010
ORDER NOW
Archive: Introduction to the FDA
October 25, 2010
ORDER NOW
Archive: Medical Device Tracking
August 18, 2010
ORDER NOW
Archive: Transitioning Pharma Professionals to Medical Device Professionals
April 5, 2010
ORDER NOW



250 First Avenue, Suite 300, Needham, MA 02494
E: customer.service@barnettinternational.com
P: 800.856.2556
P: +1 781.972.5400

About Barnett

Course Catalog

Accreditation, Policies and Procedures

Careers

FAQs

Instructor Biographies

Privacy Policy