Web Seminars for Clinical Research Professionals
A Barnett Interactive Web Seminar offers you a seamless, secure, multimedia learning experience. These live, instructor-led sessions are designed to be highly interactive and can be attended by individual attendees or groups at one low cost. No travel, no travel expenses, and no time away from the office!
-
The Fundamentals of Clinical Research Project Management The Fundamentals of Clinical Research Project Management The Fundamentals of Clinical Research Project Management
$735.00Course #: BI17049The Fundamentals of Clinical Research Project Management
February 23, 2026 |
12:00 p.m. - 1:30 p.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
16-Hour Preparing for FDA Post Marketing Adverse Drug Experience (PADE) Inspections for Pharmacovigilance 16-Hour Preparing for FDA Post Marketing Adverse Drug Experience (PADE) Inspections for Pharmacovigilance 16-Hour Preparing for FDA Post Marketing Adverse Drug Experience (PADE) Inspections for Pharmacovigilance
$2,195.00Course #: BI1705416-Hour Preparing for FDA Post Marketing Adverse Drug Experience (PADE) Inspections for Pharmacovigilance
February 24, 2026 - March 17, 2026 (Tuesday Mornings) |
* After January 24, 2026, costs are $2,195.00 11:00 a.m. - 3:00 p.m. EasternTake advantage of our $1,995.00 price by registering early!
$2,195.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank
$835.00Course #: BI17055ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank
February 24, 2026 |
12:30 p.m. - 2:30 p.m. Eastern$835.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
FDA Requirements for Electronic Source Data in Clinical Investigations FDA Requirements for Electronic Source Data in Clinical Investigations FDA Requirements for Electronic Source Data in Clinical Investigations
$735.00Course #: BI17057FDA Requirements for Electronic Source Data in Clinical Investigations
February 25, 2026 |
9:30 a.m. - 11:30 a.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
ICH E6 (R3) and ICH E8 (R1) Updates: Impact on Sponsors ICH E6 (R3) and ICH E8 (R1) Updates: Impact on Sponsors ICH E6 (R3) and ICH E8 (R1) Updates: Impact on Sponsors
$735.00Course #: BI17058ICH E6 (R3) and ICH E8 (R1) Updates: Impact on Sponsors
February 25, 2026 |
10:00 a.m. - 11:30 a.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
State Laws Governing Clinical Trial Regulatory Compliance State Laws Governing Clinical Trial Regulatory Compliance State Laws Governing Clinical Trial Regulatory Compliance
$735.00Course #: BI17056State Laws Governing Clinical Trial Regulatory Compliance
February 24, 2026 |
1:00 p.m. - 2:30 p.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
$835.00Course #: BI17059Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance
February 25, 2026 |
12:30 p.m. - 2:30 p.m. Eastern$835.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
EU Clinical Trial Regulation (EU-CTR) Requirements EU Clinical Trial Regulation (EU-CTR) Requirements EU Clinical Trial Regulation (EU-CTR) Requirements
$735.00Course #: BI17062EU Clinical Trial Regulation (EU-CTR) Requirements
February 26, 2026 |
9:00 a.m. - 10:00 a.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
FDA's Updated Informed Consent Guidance: What's New? FDA's Updated Informed Consent Guidance: What's New? FDA's Updated Informed Consent Guidance: What's New?
$835.00Course #: BI17063FDA's Updated Informed Consent Guidance: What's New?
February 26, 2026 |
9:30 a.m. - 11:00 a.m. Eastern$835.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155 Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155 Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155
$735.00Course #: BI17064Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155
February 26, 2026 |
9:30 a.m. - 11:00 a.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Negotiation Skills for Clinical Research Professionals Negotiation Skills for Clinical Research Professionals Negotiation Skills for Clinical Research Professionals
$735.00Course #: BI17061Negotiation Skills for Clinical Research Professionals
February 25, 2026 |
12:00 p.m. - 1:30 p.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
The GCPs of Essential Documents The GCPs of Essential Documents The GCPs of Essential Documents
$735.00Course #: BI17060The GCPs of Essential Documents
February 25, 2026 |
1:00 p.m. - 2:30 p.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
EU Guideline on Computerised Systems and Electronic Data in Clinical Trials EU Guideline on Computerised Systems and Electronic Data in Clinical Trials EU Guideline on Computerised Systems and Electronic Data in Clinical Trials
$835.00Course #: BI17065EU Guideline on Computerised Systems and Electronic Data in Clinical Trials
February 26, 2026 |
2:00 p.m. - 3:30 p.m. Eastern$835.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Root Cause Analysis: Applying the Concept for Better Study Compliance Management Root Cause Analysis: Applying the Concept for Better Study Compliance Management Root Cause Analysis: Applying the Concept for Better Study Compliance Management
$835.00Course #: BI17066Root Cause Analysis: Applying the Concept for Better Study Compliance Management
February 26, 2026 |
3:00 p.m. - 5:30 p.m. Eastern$835.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Electronic Informed Consent Guidance: Regulatory Updates Electronic Informed Consent Guidance: Regulatory Updates Electronic Informed Consent Guidance: Regulatory Updates
$735.00Course #: BI17068Electronic Informed Consent Guidance: Regulatory Updates
February 27, 2026 |
12:00 p.m. - 1:30 p.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Introduction to Medicare Coverage Analysis: Impact on Site Revenue Cycles Introduction to Medicare Coverage Analysis: Impact on Site Revenue Cycles Introduction to Medicare Coverage Analysis: Impact on Site Revenue Cycles
$735.00Course #: BI17072Introduction to Medicare Coverage Analysis: Impact on Site Revenue Cycles
March 2, 2026 |
9:30 a.m. - 11:30 a.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Principal Investigator Oversight and the Appropriate Delegation of Tasks Principal Investigator Oversight and the Appropriate Delegation of Tasks Principal Investigator Oversight and the Appropriate Delegation of Tasks
$735.00Course #: BI17071Principal Investigator Oversight and the Appropriate Delegation of Tasks
March 2, 2026 |
9:30 a.m. - 11:00 a.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Strategies for Remote Auditing of Investigative Sites Strategies for Remote Auditing of Investigative Sites Strategies for Remote Auditing of Investigative Sites
$1,195.00Course #: BI17070Strategies for Remote Auditing of Investigative Sites
March 2, 2026 & March 9, 2026 |
8:30 a.m. - 11:30 a.m. Eastern$1,195.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
ABCs of Clinical Research for Clinical Administrative Support Staff ABCs of Clinical Research for Clinical Administrative Support Staff ABCs of Clinical Research for Clinical Administrative Support Staff
$835.00Course #: BI17074ABCs of Clinical Research for Clinical Administrative Support Staff
March 3, 2026 |
9:00 a.m. - 11:30 a.m. Eastern$835.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Informed Consent Procedure: Lessons Learned from Inspection Findings Informed Consent Procedure: Lessons Learned from Inspection Findings Informed Consent Procedure: Lessons Learned from Inspection Findings
$735.00Course #: BI17073Informed Consent Procedure: Lessons Learned from Inspection Findings
March 2, 2026 |
1:00 p.m. - 2:30 p.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
30-Hour Design and Conduct of Clinical Trials: Requirements, Statistical Issues, and Clinical Protocols 30-Hour Design and Conduct of Clinical Trials: Requirements, Statistical Issues, and Clinical Protocols 30-Hour Design and Conduct of Clinical Trials: Requirements, Statistical Issues, and Clinical Protocols
$1,995.00Course #: BI1707730-Hour Design and Conduct of Clinical Trials: Requirements, Statistical Issues, and Clinical Protocols
March 3, 2026 - May 5, 2026 (Tuesday Evenings) |
* After February 3, 2026, costs are $1,995.00 5:30 p.m. - 8:30 p.m. EasternTake advantage of our $1,795.00 price by registering early!
$1,995.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Drug Development and FDA Regulations Drug Development and FDA Regulations Drug Development and FDA Regulations
$735.00Course #: BI17078Drug Development and FDA Regulations
March 4, 2026 |
9:00 a.m. - 12:00 p.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Implementing Quality Agreements Implementing Quality Agreements Implementing Quality Agreements
$735.00Course #: BI17079Implementing Quality Agreements
March 4, 2026 |
9:30 a.m. - 11:00 a.m. Eastern$735.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply. -
Introduction to Statistics for Non-Statisticians Introduction to Statistics for Non-Statisticians Introduction to Statistics for Non-Statisticians
$835.00Course #: BI17075Introduction to Statistics for Non-Statisticians
March 3, 2026 |
12:00 p.m. - 3:00 p.m. Eastern$835.00Please register using your academic affiliation. If academic affiliation is not provided, commercial rates will apply.
