Web Seminars - Barnett Educational Services

May 21, 2013

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JOB FUNCTION

ABCs of Clinical Research for Clinical Administrative Support Staff
May 20, 2013 | $795.00

Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
May 21, 2013 | $795.00

Essential Documentation in Clinical Trials at Research Sites
May 22, 2013 | $695.00

Final FDA Guidance: How to Complete the FDA Form 1572, Adequately and Accurately
May 23, 2013 | $595.00

Writing and Maintaining the EU Clinical Trial Authorization
May 24, 2013 | $795.00

Quality Risk Management in Clinical Trials and Pharmacovigilance
May 30, 2013 | $695.00

Regulatory Intelligence
May 31, 2013 | $695.00

Writing and Updating the Investigator's Brochure
June 3, 2013 | $795.00

Good Clinical Practice: Practical Application and Implementation
June 7, 2013 | $795.00

Informed Consent Content & Process Requirements
June 10, 2013 | $595.00

Principal Investigator (PI) Oversight and the Appropriate Delegation of Tasks
June 13, 2013 | $695.00

10-Week Clinical Research Associate (CRA) On-Boarding Program
June 14 - August 23, 2013 | $1,895.00

NEW! Biosimilar Products: An Introduction to Approval Pathways
June 14, 2013 | $695.00

GCP Training for Investigators
June 20, 2013 | $795.00

Drug Development and FDA Regulations
June 20, 2013 | $695.00

Use of Notes to File in Clinical Trial Essential Documentation
June 24, 2013 | $795.00

Adverse Event Monitoring for CRAs
June 28, 2013 | $695.00

Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
July 12, 2013 | $795.00

Use of Notes to File in Clinical Trial Essential Documentation
July 16, 2013 | $795.00

Investigator Initiated Trials: Roles and Responsibilities
July 17, 2013 | $695.00

Electronic Medical Records: Approaches for Ensuring Source Document and 21 CFR Part 11 Required Components
July 17, 2013 | $795.00

Final FDA Guidance: How to Complete the FDA Form 1572, Adequately and Accurately
July 18, 2013 | $595.00

Good Clinical Practice: Practical Application and Implementation
July 22, 2013 | $795.00

ABCs of Clinical Research for Clinical Administrative Support Staff
July 23, 2013 | $795.00

Final AE Regulatory Guidance: Reporting/Communication of Safety Information from Clinical Trials to IRBs
July 25, 2013 | $595.00

10 Week CRA & CRC: Beginner Program
July 25 - September 26, 2013 | Register by June 24 for only $1,695.00

The IND in a CTD/eCTD Format
July 26, 2013 | $695.00

Writing Clinical Study Protocols
July 29, 2013 | $795.00

CRA Current Practice Update: Impact of the FDA BIMO Program
August 1, 2013 | $695.00

Introduction to Data Management
August 2, 2013 | $695.00

The IND in a CTD/eCTD Format
August 5, 2013 | $695.00

Electronic Medical Records: Approaches for Ensuring Source Document and 21 CFR Part 11 Required Components
August 13, 2013 | $795.00

Risk-Based Monitoring: The Data Management Connection
August 16, 2013 | $695.00

Principal Investigator (PI) Oversight and the Appropriate Delegation of Tasks
August 20, 2013 | $695.00

10 Week CRA & CRC: Beginner Program
August 21 - October 23, 2013 | Register by July 19 for only $1,695.00

Changes and Challenges in Foreign Clinical Research
August 22, 2013 | $695.00

NEW! Clinical Trials and the Sunshine Act: The Effect on the Clinical Research Industry
August 22, 2013 | $695.00

NEW! Understanding Global Requirements for Trial Registration and Disclosure of Results
August 23, 2013 | $695.00

Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
August 27, 2013 | $795.00

Writing and Maintaining the EU Clinical Trial Authorization
September 9, 2013 | $795.00

ABCs of Clinical Research for Clinical Administrative Support Staff
September 9, 2013 | $795.00

Pediatric Clinical Drug Development
September 10, 2013 | $695.00

Negotiation Skills for Clinical Research Professionals
September 10, 2013 | $695.00

Drug Safety and Pharmacovigilance
September 11, 2013 | $695.00

Good Clinical Practice: Practical Application and Implementation
September 13, 2013 | $795.00

Fraud in Clinical Research: An Overview
September 13, 2013 | $795.00

Investigator Initiated Trials: Roles and Responsibilities
September 16, 2013 | $695.00

Writing and Updating the Investigator's Brochure
September 16, 2013 | $795.00

Case Report Form Design, Strategy, and Standards Workshop
September 17, 2013 | Register by August 16 for only $800.00

Biosimilar Products: An Introduction to Approval Pathways
September 17, 2013 | $695.00

Study Site Start-Up: Organization and Management Tips for the Novice Clinical Research Site
September 18, 2013 | $595.00

Developing and Negotiating Research Site Clinical Study Budgets and Contracts
September 19, 2013 | $795.00

NEW! Leading Teams in a Changing Clinical Research Environment
September 19, 2013 | $695.00

10-Week Clinical Research Associate (CRA) On-Boarding Program
September 20 - November 22, 2013 | Register by August 19 for only $1,695.00

Drug Development and FDA Regulations
September 20, 2013 | $695.00

NEW! Writing Protocols for Diagnostic Studies
September 25, 2013 | $695.00

Data Quality in Clinical Trials: Rationale and Impact
September 25, 2013 | $695.00

FDA Meetings: Drugs and Biologics
September 25, 2013 | $695.00

Subject Recruitment: Proactive Project Plans & Issues Management
September 30, 2013 | $595.00

Use of Notes to File in Clinical Trial Essential Documentation
October 1, 2013 | $795.00

Writing Clinical Study Protocols
October 1, 2013 | $795.00

Good Clinical Practice: Practical Application and Implementation
October 2, 2013 | $795.00

Recent Trends in Noncompliance: Critical Review and Analysis of Recent Regulatory Letters and Communications from the FDA, EMA, and Health Canada
October 3, 2013 | $695.00

Critical Decision Points in Design & Conduct of Patient Registries
October 4, 2013 | $795.00

Quality Risk Management in Clinical Trials and Pharmacovigilance
October 8, 2013 | $695.00

Introduction to Signal Detection and Data Mining
October 9, 2013 | $795.00

10 Week CRA & CRC: Beginner Program
October 10 - December 19, 2013 | Register by September 6 for only $1,695.00

CRC & PI Current Practice Update: Impact of the FDA BIMO Program
October 11, 2013 | $595.00

Worldwide Orphan Drug Designation Applications and Requirements
October 14, 2013 | $695.00

NEW! Writing the Clinical Study Report
October 17, 2013 | $695.00

NEW! Writing Clinical Study Reports for Diagnostic Studies
October 17, 2013 | $695.00

Developing and Negotiating Research Site Clinical Study Budgets and Contracts
October 18, 2013 | $795.00

NEW! Data Management in the Electronic Data Capture Arena
October 18, 2013 | $695.00

Corrective Action Plans: Essential Documentation of a Site's Response to GCP Deficiencies
October 21, 2013 | $795.00

Updates in Informed Consent Guidance
October 22, 2013 | $695.00

Regulatory 101: Navigating the Background, Laws, and Pertinent Regulations
October 24, 2013 | $695.00

FDA Drug Approval Process
October 24, 2013 | $695.00

Adverse Event Monitoring for CRAs
October 25, 2013 | $695.00

HIPAA Team Training: Fundamental Training Specifically for Clinical Research Settings
October 28, 2013 | $595.00

GCP Training for Investigators
October 28, 2013 | $795.00

Preparing Clinical Research Sites for FDA Inspections
October 29, 2013 | $595.00

Human Subject Protection: DHHS and the FDA
October 30, 2013 | $695.00

FDA Guidance: IRB Continuing Review of Clinical Investigations
November 1, 2013 | $695.00

Final AE Regulatory Guidance: Reporting/Communication of Safety Information from Clinical Trials to IRBs
November 4, 2013 | $595.00

Regulatory Intelligence
November 6, 2013 | $695.00

10 Week CRA & CRC: Beginner Program
November 6, 2013 - January 29, 2014 | Register by October 4 for only $1,695.00

Risk-Based Monitoring: The Data Management Connection
November 8, 2013 | $695.00

CRA Current Practice Update: Impact of the FDA BIMO Program
November 12, 2013 | $695.00

Managing CRAs to Improve Performance & Study Outcomes
November 13, 2013 | $595.00

Introduction to Data Management
November 13, 2013 | $695.00

Developing and Negotiating Research Site Clinical Study Budgets and Contracts
November 14, 2013 | $795.00

The IND in a CTD/eCTD Format
November 14, 2013 | $695.00

NEW! Clinical Trials and the Sunshine Act: The Effect on the Clinical Research Industry
November 18, 2013 | $695.00

Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
November 19, 2013 | $795.00

CRC Role/Responsibilities Training
November 19, 2013 | $595.00

NEW! Understanding Global Requirements for Trial Registration and Disclosure of Results
November 20, 2013 | $695.00

Changes and Challenges in Foreign Clinical Research
November 21, 2013 | $695.00

ABCs of Clinical Research for Clinical Administrative Support Staff
November 25, 2013 | $795.00

Use of Notes to File in Clinical Trial Essential Documentation
November 26, 2013 | $795.00

Essential Documentation in Clinical Trials at Research Sites
November 26, 2013 | $695.00

Investigator Initiated Trials: Roles and Responsibilities
December 2, 2013 | $695.00

Good Clinical Practice: Practical Application and Implementation
December 4, 2013 | $795.00

Principal Investigator (PI) Oversight and the Appropriate Delegation of Tasks
December 5, 2013 | $695.00

10-Week Clinical Research Associate (CRA) On-Boarding Program
December 6, 2013 - February 21, 2014 | Register by November 4 for only $1,695.00

Electronic Medical Records: Approaches for Ensuring Source Document and 21 CFR Part 11 Required Components
December 6, 2013 | $795.00

Fraud in Clinical Research: An Overview
December 10, 2013 | $795.00

Pediatric Clinical Drug Development
December 10, 2013 | $695.00

Use of Notes to File in Clinical Trial Essential Documentation
December 11, 2013 | $795.00

NEW! Writing Protocols for Diagnostic Studies
December 11, 2013 | $695.00

Writing and Maintaining the EU Clinical Trial Authorization
December 12, 2013 | $795.00

Drug Development and FDA Regulations
December 17, 2013 | $695.00

Writing and Updating the Investigator's Brochure
December 18, 2013 | $795.00

Final FDA Guidance: How to Complete the FDA Form 1572, Adequately and Accurately
December 18, 2013 | $595.00

Biosimilar Products: An Introduction to Approval Pathways
December 19, 2013 | $695.00

Data Quality in Clinical Trials: Rationale and Impact
December 20, 2013 | $695.00

Case Report Form Design, Strategy, and Standards Workshop
January 7, 2014 | Register by December 6 for only $800.00

Writing Clinical Study Protocols
January 8, 2014 | $795.00

NEW! Leading Teams in a Changing Clinical Research Environment
January 8, 2014 | $695.00

Corrective Action Plans: Essential Documentation of a Site's Response to GCP Deficiencies
January 13, 2014 | $795.00

Recent Trends in Noncompliance: Critical Review and Analysis of Recent Regulatory Letters and Communications from the FDA, EMA, and Health Canada
January 13, 2014 | $695.00

Human Subject Protection: DHHS and the FDA
January 14, 2014 | $695.00

Negotiation Skills for Clinical Research Professionals
January 14, 2014 | $695.00

Developing and Negotiating Research Site Clinical Study Budgets and Contracts
January 16, 2014 | $795.00

NEW! Data Management in the Electronic Data Capture Arena
January 21, 2014 | $695.00

Quality Risk Management in Clinical Trials and Pharmacovigilance
January 21, 2014 | $695.00

10 Week CRA & CRC: Beginner Program
January 23 - March 27, 2014 | Register by December 20 for only $1,695.00

Adverse Event Monitoring for CRAs
January 24, 2014 | $695.00

Use of Notes to File in Clinical Trial Essential Documentation
January 27, 2014 | $795.00

NEW! Writing Clinical Study Reports for Diagnostic Studies
January 30, 2014 | $695.00

NEW! Writing the Clinical Study Report
January 30, 2014 | $695.00

On-Demand GCP Refresher Training

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
For details on our scenario-based practical GCP application on-demand course, click here.

Barnett "Hands-On" Workshops are designed to provide intensive, hands-on training in a highly targeted clinical research topic area in a very interactive and engaging learning environment. To view more details and available courses, click here.

BARNETT CATALOGThe Barnett Catalogue is your comprehensive guide to the myriad live, web, and custom training opportunities offered throughout the year.

Jan - Jul 2013 Edition

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