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UPCOMING LIVE SEMINARS
Clinical Project Management: Fundamentals of Project Management
June 7-8, 2021
Boston, MA
Monitoring Clinical Drug Studies: Beginner
June 9-11, 2021
Boston, MA
CRA & CRC: Beginner Program
June 14-16, 2021
San Diego, CA
Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) in Site Management
June 16-17, 2021
San Diego, CA
Search Results -
Publications
Biologics Development: A Regulatory Overview (2004)
Glossary Acronyms for Clinical Research Professionals
HIPAA and U.S. Clinical Trials: A Question & Answer Reference Guide 2014
The Form FDA 1572: A Reference Guide for Clinical Researchers, Sponsors, and Monitors
CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)
CRA Training Series: Volume 1 - An Overview of Drug Development (2018)
CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)
CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)
CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)
CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)
CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)
CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)
The Clinical Research Finance Roadmap: A Comprehensive Guide to the Financial Aspects of Clinical Research
The Clinical Research Finance Roadmap Companion Reference Guide: Tools, Templates and Resources
Live Seminars
No results found. Unable to find what you were looking for? Contact Melissa Dolen at 781-972-5418 to discuss your options and take advantage of the savings.
mdolen
@healthtech.com
Web Seminars
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Final ICH GCP E6 R2: Changes Impacting Sponsors/CROs
January 29, 2021 | Interactive Web Seminar
Final ICH GCP E6 R2: Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsors-Investigators and Institutions)
January 29, 2021 | Interactive Web Seminar
Introduction to Medicare Coverage Analysis: Impact on Site Revenue Cycles
February 8, 2021 | Interactive Web Seminar
Final ICH GCP E6 R2 Addendum: Overview of Changes Impacting Sponsors, CROs, Clinical Investigators/Sites
February 9, 2021 | Interactive Web Seminar
Current FDA and EMA Inspection Findings: Lessons Learned
February 10, 2021 | Interactive Web Seminar
Scientific and Ethical Considerations for Inclusion of Pregnant Women in Clinical Trials
February 15, 2021 | Interactive Web Seminar
ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank
February 17, 2021 | Interactive Web Seminar
Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155
February 18, 2021 | Interactive Web Seminar
30-Hour Clinical Research Auditing Certification Program
February 18 - April 29, 2021 | Interactive Web Seminar
Introduction to Clinical Research
February 19, 2021 | Interactive Web Seminar
EMA and MHRA Inspections: Successful Planning and Execution Tips and Techniques
February 22, 2021 | Interactive Web Seminar
Investigational Product Accountability Best Practices
February 26, 2021 | Interactive Web Seminar
Introduction to Statistics for Non-Statisticians
March 2, 2021 | Interactive Web Seminar
10-Week Final ICH GCP E6 R2: Risk-Based Monitoring Plan Development Series
March 2 - May 4, 2021 | Interactive Web Seminar
ABCs of GCP and the 13 Principles of ICH GCP E6
March 3, 2021 | Interactive Web Seminar
10-Week Risk Management/Risk-Based Quality Management for Clinical Trials Certification Program
March 5 - May 7, 2021 | Interactive Web Seminar
Electronic Informed Consent Guidance: Regulatory Updates
March 9, 2021 | Interactive Web Seminar
Civil Money Penalties Relating to the ClinicalTrials.gov Data Bank: Final Guidance
March 11, 2021 | Interactive Web Seminar
FDA Medical Device Approval Process
March 12, 2021 | Interactive Web Seminar
Clinical Research Financial Management for Investigative Sites
March 18, 2021 | Interactive Web Seminar
Archived Web Seminars
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Archive: Introduction to Clinical Research
November 17, 2020 •
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Archive: TMF/eTMF Regulatory Agency Expectations, Inspections, and Findings
October 16, 2020 •
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Archive: Final ICH GCP E6 R2: Implementing Risk Management Approaches for Compliance
October 14, 2020 •
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Archived: The Revised HHS Common Rule: What You Need to Know Now
September 18, 2020 •
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Archive: eTMF Quality Oversight: A Risk-Based Approach
September 11, 2020 •
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Archive: Final ICH GCP E6 R2: Sponsor Quality Management - Risk-Based/Risk Management Requirements and Approaches for Compliance
July 21, 2020 •
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Archive: CAP and CLIA Requirements for Clinical Research Laboratories
May 12, 2020 •
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Archive: Introduction to Medicare Coverage Analysis: Impact on Site Revenue Cycles
May 7, 2020 •
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Single Copy - $735.00
Archive: Centralized TMF Management: The CRO Sponsor Partnership
April 24, 2020 •
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Archive: Investigational Product Accountability Best Practices
April 23, 2020 •
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Archive: Writing the Clinical Study Report
January 15, 2020 •
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Archive: Final ICH GCP E6 R2 Addendum: Overview of Changes Impacting Sponsors, CROs, Clinical Investigators/Sites
December 19, 2019 •
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Site License - $1,835.00
Archive: EMA and MHRA Inspections: Successful Planning and Execution Tips and Techniques
December 19, 2019 •
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Single Copy - $945.00
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Archive: Sponsor Responsibilities for Global Drug Studies
December 17, 2019 •
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Archive: Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155
December 4, 2019 •
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Site License - $1,735.00
Archive: Introduction to Statistics for Non-Statisticians
November 18, 2019 •
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Site License - $1,835.00
Archive: Informed Consent Procedure: Lessons Learned from Inspection Findings
November 4, 2019 •
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Archive: State Laws Governing Clinical Trial Regulatory Compliance
September 25, 2019 •
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Archive: TMF/eTMF Audit Strategies
September 20, 2019 •
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Archive: Use of Electronic Health Record Data in Clinical Investigations
September 18, 2019 •
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