e6 ich guidelines

Results

Clinical Research Resources, LLC

Book 1B: 2026 FDA Good Clinical Practice Guide (With FDA/ICH GCP E6(R3))

$26.95

GMP

ICH E6(R3) - Good Clinical Practice

$7.90

GuideGxP

ICH Efficacy Guidelines E – Clinical Studies, GCP, E6(R3) & Global Structure

$106.00

Clinical Research Resources, LLC

Book 1A-FDAE6R3: 2025 Selected Regulations & Guidance for Drug Studies (With FDA/ICH GCP E6(R3))

$24.95

Barnett International

Archive: ICH E6 (R3) Draft: A Discussion

$835.00

Barnett International

Good Clinical Practice for Sponsors & Service Providers (ICH E6 R3)

$199.00

Barnett International

Archive: Final ICH GCP E6 R2: Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsors-Investigators and Institutions)

$835.00

Barnett International

Good Clinical Practice for Investigators and Coordinators (ICH E6 R3)

$199.00

Barnett International

Archive: Understanding ICH E6(R3) (GCP) Updates: Key Changes from R2

$835.00

Barnett International

Archive: ICH GCP E6(R3) Updates: Key Changes Impacting Sponsors and CROs

$835.00

Archive: ICH GCP E6 R2 and R3 Updates: Implementing Risk Management Approaches for Compliance

Barnett International

Archive: ICH GCP E6(R3) Updates: Implementing Risk Management Approaches for Compliance

$835.00

Barnett International

Archive: Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155

$735.00

Barnett International

Archive: ICH GCP E6(R3) Updates: Overview of Changes Impacting Sponsors, CROs, and Clinical Investigators/Sites

$835.00

Barnett International

Archive: ICH E6(R3) and ICH E8(R1) Updates: Impact on Sponsors

$735.00

Barnett International

Archive: ABCs of GCP and the 13 Principles of ICH GCP E6

$735.00

Clinical Research Resources, LLC

Book 1A: 2026 Selected Regulations & Guidance for Drug Studies (With FDA/ICH GCP E6(R3))

$25.95

Clinical Research Resources, LLC

Book 1C: 2026 Good Clinical Practice Regulations in the US & the EU (With FDA/ICH GCP E6(R3))

$25.95

Barnett International

Fundamentals of Good Clinical Practice (ICH E6 R3)

$199.00

Clinical Research Resources, LLC

Book CG1: 2026 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials (With FDA/ICH GCP E6(R3))

$46.95

Clinical Research Resources, LLC

Book 1B-FDAE6R3: 2025 FDA Good Clinical Practice Guide (With FDA/ICH GCP E6(R3))

(1)

$26.95

GMP

Good Clinical Practice Handbook

$13.95

Barnett International

Archive: Writing and Updating the Investigator's Brochure

$835.00

Barnes & Noble

Practical Guide to Clinical Data Management

$180.00

Triticon

Oversight in Clinical Development

(2)

$60.00

GMP

Medical Device Clinical with EU Directive

$18.95

Barnett International

Archive: GCP Renovation (ICH E8 R1 and ICH E6 R3)

$835.00

GMP

21 CFR 11, 58, 210/211, 820, ICH E6(R3) - GMP 2

$11.95

GMP

GCLP Good Clinical Laboratory Handbook - 4.5x7.5

$29.95

Barnett International

Biologics Development: A Regulatory Overview (2021)

$195.00

Barnett International

Good Clinical Practice: A Question & Answer Reference Guide 2024/2025

$139.00

Results

Book 1B: 2026 FDA Good Clinical Practice Guide <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

ICH E6(R3) - Good Clinical Practice

ICH Efficacy Guidelines E – Clinical Studies, GCP, E6(R3) & Global Structure

Book 1A-FDAE6R3: 2025 Selected Regulations & Guidance for Drug Studies <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Archive: ICH E6 (R3) Draft: A Discussion

Good Clinical Practice for Sponsors & Service Providers (ICH E6 R3)

Archive: Final ICH GCP E6 R2: Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsors-Investigators and Institutions)

Good Clinical Practice for Investigators and Coordinators (ICH E6 R3)

Archive: Understanding ICH E6(R3) (GCP) Updates: Key Changes from R2

Archive: ICH GCP E6(R3) Updates: Key Changes Impacting Sponsors and CROs

Archive: ICH GCP E6(R3) Updates: Implementing Risk Management Approaches for Compliance

Archive: Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155

Archive: ICH GCP E6(R3) Updates: Overview of Changes Impacting Sponsors, CROs, and Clinical Investigators/Sites

Archive: ICH E6(R3) and ICH E8(R1) Updates: Impact on Sponsors

Archive: ABCs of GCP and the 13 Principles of ICH GCP E6

Book 1A: 2026 Selected Regulations & Guidance for Drug Studies <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Book 1C: 2026 Good Clinical Practice Regulations in the US & the EU <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Fundamentals of Good Clinical Practice (ICH E6 R3)

Book CG1: 2026 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Book 1B-FDAE6R3: 2025 FDA Good Clinical Practice Guide <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Good Clinical Practice Handbook

Archive: Writing and Updating the Investigator's Brochure

Practical Guide to Clinical Data Management

Oversight in Clinical Development

Medical Device Clinical with EU Directive

Archive: GCP Renovation (ICH E8 R1 and ICH E6 R3)

21 CFR 11, 58, 210/211, 820, ICH E6(R3) - GMP 2

GCLP Good Clinical Laboratory Handbook - 4.5x7.5

Biologics Development: A Regulatory Overview (2021)

Good Clinical Practice: A Question & Answer Reference Guide 2024/2025

Results

Book 1B: 2026 FDA Good Clinical Practice Guide <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

ICH E6(R3) - Good Clinical Practice

ICH Efficacy Guidelines E – Clinical Studies, GCP, E6(R3) &amp; Global Structure

Book 1A-FDAE6R3: 2025 Selected Regulations & Guidance for Drug Studies <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Archive: ICH E6 (R3) Draft: A Discussion

Good Clinical Practice for Sponsors & Service Providers (ICH E6 R3)

Archive: Final ICH GCP E6 R2: Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsors-Investigators and Institutions)

Good Clinical Practice for Investigators and Coordinators (ICH E6 R3)

Archive: Understanding ICH E6(R3) (GCP) Updates: Key Changes from R2

Archive: ICH GCP E6(R3) Updates: Key Changes Impacting Sponsors and CROs

Archive: ICH GCP E6(R3) Updates: Implementing Risk Management Approaches for Compliance

Archive: Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155

Archive: ICH GCP E6(R3) Updates: Overview of Changes Impacting Sponsors, CROs, and Clinical Investigators/Sites

Archive: ICH E6(R3) and ICH E8(R1) Updates: Impact on Sponsors

Archive: ABCs of GCP and the 13 Principles of ICH GCP E6

Book 1A: 2026 Selected Regulations & Guidance for Drug Studies <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Book 1C: 2026 Good Clinical Practice Regulations in the US & the EU <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Fundamentals of Good Clinical Practice (ICH E6 R3)

Book CG1: 2026 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Book 1B-FDAE6R3: 2025 FDA Good Clinical Practice Guide <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>

Good Clinical Practice Handbook

Archive: Writing and Updating the Investigator's Brochure

Practical Guide to Clinical Data Management

Oversight in Clinical Development

Medical Device Clinical with EU Directive

Archive: GCP Renovation (ICH E8 R1 and ICH E6 R3)

21 CFR 11, 58, 210/211, 820, ICH E6(R3) - GMP 2

GCLP Good Clinical Laboratory Handbook - 4.5x7.5

Biologics Development: A Regulatory Overview (2021)

Good Clinical Practice: A Question & Answer Reference Guide 2024/2025

ICH Efficacy Guidelines E – Clinical Studies, GCP, E6(R3) & Global Structure