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SAVE 50% on the purchase of a Web Seminar Archive during the month of June! Use Promo Code JUN19 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: RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials
June 20, 2019
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Archive: Establishing Quality Tolerance Limits
June 18, 2019
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Archive: Final ICH GCP E6 R2 Addendum: Overview of Changes Impacting Sponsors, CROs, Clinical Investigators/Sites
June 13, 2019
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Archive: Preparing Clinical Research Sites for FDA Inspections
June 12, 2019
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Archive: Risk-Based Site Monitoring
June 11, 2019
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Archive: The Revised HHS Common Rule: What You Need to Know Now
June 10, 2019
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Archive: FDA Drug Approval Process
June 3, 2019
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Archive: Trial Master File (TMF) for Sponsors: Set-Up and Maintenance
May 31, 2019
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Archive: Developing and Negotiating Research Site Clinical Study Budgets and Contracts
May 30, 2019
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Archive: Risk-Based Monitoring: The Data Management Connection
May 29, 2019
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Archive: Clinical Trial Start-Up: Using a Work Breakdown Structure (WBS) for Effective Planning
May 23, 2019
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Archive: Leading Teams in a Changing Clinical Research Environment
May 22, 2019
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Archive: Regulatory Intelligence
May 22, 2019
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Archive: ABCs of GCP and the 13 Principles of ICH GCP E6
May 10, 2019
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Archive: Root Cause Analysis: Applying the Concept for Better Study Compliance Management
May 9, 2019
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Archive: Corrective Action Plans: Essential Documentation of a Site's Response to GCP Deficiencies
May 2, 2019
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Archive: Current FDA and EMA Inspection Findings: Lessons Learned
May 2, 2019
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Archive: CAP and CLIA Requirements for Clinical Research Laboratories
May 1, 2019
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Archive: Monitoring Visit Reports for Medical Device Studies
April 30, 2019
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Archive: FDA's Bioresearch Monitoring (BIMO) Program: Inspection of Sponsors, CROs, and Monitors
April 30, 2019
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Archive: Monitoring Medical Device Trials: An Introduction
April 29, 2019
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Archive: Case Report Form Design, Strategy, and Standards
April 24, 2019
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Archive: Final ICH GCP E6 R2: Implementing Risk Management Approaches for Compliance
April 22, 2019
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Archive: Protocol Deviations: Documenting, Managing, and Reporting
April 18, 2019
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Archive: Data Quality in Clinical Trials: Rationale and Impact
April 17, 2019
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Archive: Risk-Based Thinking: How Monitors Can Develop an Auditor's Perspective
April 12, 2019
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Archive: Good Clinical Practice: Practical Application and Implementation
April 11, 2019
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Archive: ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank
April 10, 2019
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Archive: Medical Writing Fundamentals: How to Write Regulatory Documents
April 10, 2019
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Archive: Investigator Initiated Trials: Roles and Responsibilities
April 9, 2019
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Archive: Ensuring Success Through Smarter Site Selection and Study Feasibility
April 4, 2019
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Archive: Strategies for Having Difficult Conversations
March 26, 2019
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Archive: Final ICH GCP E6 R2: Sponsor Quality Management - Risk-Based/Risk Management Requirements and Approaches for Compliance
March 21, 2019
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Archive: Building Relationships with Clinical Research Sites
March 20, 2019
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Archive: Principal Investigator Oversight and the Appropriate Delegation of Tasks
March 19, 2019
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Archive: Monitoring Reports: 10 Rules of Effective Report Writing
March 18, 2019
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Archive: Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
March 18, 2019
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Archive: Monitoring Plan Development
February 21, 2019
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Archive: Implementing Quality Agreements
February 12, 2019
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Archive: Coaching Skills for Leaders
February 7, 2019
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Archive: Cases in Advanced GCP: A Problem-Solving Practicum
February 7, 2019
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Archive: Final ICH GCP E6 R2: Impact on Clinical Data Management
January 30, 2019
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Archive: Writing the Clinical Study Report
January 23, 2019
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Archive: Introduction to Data Management
January 23, 2019
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Archive: The GCPs of Essential Documents
January 21, 2019
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Archive: Adverse Event Monitoring for CRAs
January 16, 2019
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Archive: Introduction to Statistics for Non-Statisticians
December 18, 2018
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Archive: The CRA Role in Risk-Based Monitoring: Strategies for Effective Remote Monitoring
December 17, 2018
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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
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Archive: Use of Notes to File in Clinical Trial Essential Documentation
November 13, 2018
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Archive: Auditing Sponsors and CROs: Deconstruction and Application of the FDA's Compliance Program Guidance Manual
November 5, 2018
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Archive: Final ICH GCP E6 R2: Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsors-Investigators and Institutions)
October 22, 2018
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Archive: Introduction to Clinical Research
October 1, 2018
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Archive: TMF/eTMF Audit Strategies
September 14, 2018
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Archive: Strategies for Managing Difficult Clinical Research Sites
September 6, 2018
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Archive: Subject Recruitment: Proactive Project Plans and Issues Management
July 20, 2018
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Archive: Use of Electronic Health Record Data in Clinical Investigations
June 28, 2018
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Archive: Source Documentation: What is Adequate and Accurate?
June 25, 2018
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Archive: Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155
June 25, 2018
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Archive: Managing CRAs to Improve Performance and Study Outcomes
June 21, 2018
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Archive: EMA and MHRA Inspections: Successful Planning and Execution Tips and Techniques
June 12, 2018
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Archive: Preparation, Management, and Response to Inspections and Audits
June 5, 2018
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Archive: Monitoring Oncology Clinical Trials
May 23, 2018
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Archive: Electronic Medical Records: Approaches for Ensuring Source Document and 21 CFR Part 11 Required Components
May 17, 2018
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Archive: Informed Consent Procedure: Lessons Learned from Inspection Findings
May 15, 2018
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Archive: TMF/eTMF Regulatory Agency Expectations, Inspections, and Findings
May 11, 2018
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Archive: Data Management Plan Creation: Content and Rationale
May 9, 2018
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Archive: Writing and Updating the Investigator's Brochure
May 9, 2018
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Archive: Final ICH GCP E6 R2: Changes Impacting Sponsors/CROs
May 8, 2018
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Archive: FDA Medical Device Approval Process
May 7, 2018
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Archive: Tools for Trainers: Clinical Research Job-Aids and Checklists
May 2, 2018
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Archive: ABCs of Clinical Research for Clinical Administrative Support Staff
May 1, 2018
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Archive: CRA Current Practice Update: Impact of the FDA Bioresearch Monitoring (BIMO) Program
April 26, 2018
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Archive: The IND in a CTD/eCTD Format
April 25, 2018
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Archive: HIPAA Team Training: Fundamental Training Specifically Clinical Research Settings
April 23, 2018
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Archive: Developing Clinical Study Budgets for Sponsors
March 16, 2018
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Archive: Approaches to Address Challenges in Vendor Management
March 15, 2018
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Archive: eTMF Quality Oversight: A Risk-Based Approach
March 9, 2018
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Archive: Adequate Sponsor Monitoring Systems In Anticipation of FDA Sponsor GCP Inspections
January 30, 2018
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Archive: Writing Clinical Study Protocols
January 17, 2018
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Archive: Drug Development and FDA Regulations
December 13, 2017
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Archive: CRO Partnership Management
November 22, 2017
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Archive: Writing and Maintaining the EU Clinical Trial Authorization
November 8, 2017
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Archive: Recent Trends in Noncompliance: Critical Review and Analysis
November 1, 2017
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Archive: Electronic Source Data in Clinical Investigations
August 24, 2017
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Archive: Managing Risks in Outsourced Clinical Trials
August 22, 2017
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Archive: eTMF Implementation Strategies
June 2, 2017
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Archive: Data Management in the Electronic Data Capture Arena
April 11, 2017
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Archive: Case Narrative Writing for Reporting Adverse Events
March 23, 2017
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Archive: Final AE Regulatory Guidance
March 13, 2017
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Archive: Centralized TMF Management: The CRO Sponsor Partnership
March 10, 2017
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Archive: Essential Documentation in Clinical Trials at Research Sites
March 2, 2017
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Archive: Quality by Design in Clinical Research: Is This Only for the Protocol?
December 7, 2016
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Archive: Fraud in Clinical Research: An Overview
November 9, 2016
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Archive: Risk-Based Auditing: Effective Compliance Strategies
October 31, 2016
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Archive: EMA and FDA Inspections: Key Differences and Similarities
October 25, 2016
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Archive: Final FDA Guidance: How to Complete the Form FDA 1572
October 3, 2016
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Archive: CRO Selection Criteria, Eval, & Establishing the Relationship
September 16, 2016
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Archive: Establishing a Risk Management Framework for Clin Trial Conduct
August 24, 2016
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Archive: Investigational Product Accountability Best Practices
July 20, 2016
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Archive: Detecting Risk Signals in Protocols, Data, and Monitoring
July 19, 2016
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Archive: Quality Systems: A Controlled Approach to GCP Compliance
May 19, 2016
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Archive: Re-Engineering the RFP and Bid Defense Meeting
May 4, 2016
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Archive: Annual GCP Training Update: MHRA Inspection Findings for 2015
February 29, 2016
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Archive: Subject Enrollment: Creating Effective Enrollment Models
February 8, 2016
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Archive: Principal Investigator/Site GCP Compliance and Performance
February 3, 2016
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Archive: Data Management: Key Regulations Impacting the Role of the CDM
January 12, 2016
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Archive: SDTM and CDASH: What's the Connection?
January 12, 2016
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Archive: Quality Risk Management in Clinical Trials and Pharmacovigilance
December 10, 2015
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Archive: Study Feasibility: Eliminating Low and Late Enrollment
November 24, 2015
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Archive: Sponsor Management of Investigator Non-Compliance
November 20, 2015
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Archive: Establishing a Vendor Management Program
November 16, 2015
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Archive: Clinical Trials and the Sunshine Act
November 3, 2015
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Archive: Sponsor Responsibilities for Global Drug Studies
October 5, 2015
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Archive: Critical Decision Points in Design and Conduct of Patient Reg.
September 17, 2015
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Archive: Strategies for Developing Effective Training & Facilitation Skills
July 23, 2015
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Archive: Strategies for Ensuring Good Documentation Practices (GDP)
June 25, 2015
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Archive: Principal Investigator Training: Roles and Responsibilities
May 18, 2015
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Archive: Improving Readability of SOPs and Other Procedural Documents
May 5, 2015
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Archive: Writing Protocols for Diagnostic Studies
April 15, 2015
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Archive: Strategies for Conducting Vendor Audits
April 3, 2015
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Archive: Quality by Design: A Lean Six Sigma Approach to Risk-Based Mon.
March 24, 2015
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Archive: Study Initiation Strategies for Sponsors: Study and Site Start-Up
March 13, 2015
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Archive: State Laws Governing Clinical Trial Regulatory Compliance
February 24, 2015
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Archive: Risk-Based Monitoring for Sites: Prepare Your Site for Success
December 1, 2014
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Archive: Social Media in Clinical Research
August 22, 2014
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Archive: Auditor Emotional Intelligence
June 11, 2014
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Archive: Monitoring Phase I Clinical Trials
May 23, 2014
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Archive: Study Site Start-Up: Organization and Management Tips
May 6, 2014
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Archive: Phase I Study Management
April 11, 2014
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Archive: Writing Quality SOPs:Guidelines, Tools, Templates for SOP Creation
March 21, 2014
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Archive: Strategies for Protocol Operationalization and Adherence
March 17, 2014
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Archive: Real-World Monitoring: Tips for Success and Sanity
January 16, 2014
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Archive: Preparing for SOP Inspection: An Auditor's Perspective
December 5, 2013
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Archive: Writing Clinical Study Reports for Diagnostic Studies
October 17, 2013
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Archive: GCP Training for Investigators
June 20, 2013
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Archive: Informed Consent Content & Process Requirements
June 10, 2013
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Archive: Managing Observational Studies
August 23, 2012
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Archive: Writing SOPs and Procedural Documents
August 22, 2012
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Archive: Design Considerations for GCP Training Programs
May 2, 2012
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Archive: CRC Role/Responsibilities Training
April 24, 2012
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Archive: Implementation of Procedural Documents
March 16, 2012
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Archive: Five Key Strategic Steps for Developing Global SOPs
March 1, 2012
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Archive: SOP on SOPs and Procedural Document Templates
February 20, 2012
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Archive: Procedural Document System: Organized Development
February 1, 2012
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Companion Diagnostics
August 24-25, 2011
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Archive: Site Management and the Art of Assertiveness
March 24, 2011
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Archive: Making Good Teams Better: Taking Your Cross-Functional Global Team
November 11, 2010
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Archive: Presentation Skills Training for Clinical Research Professionals
November 9, 2010
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Archive: Introduction to the FDA
October 25, 2010
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Archive: Medical Device Tracking
August 18, 2010
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Archive: Transitioning Pharma Professionals to Medical Device Professionals
April 5, 2010
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