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GCP Questions, FDA Answers 2023 Edition

GCP Questions, FDA Answers, 2023 Edition

$397.00
Gain peace of mind in your next clinical trial with answers to your most pressing compliance questions, and answers to those you might not have even thought of yet, in GCP Questions, FDA Answers. Read More

Books

Tracking the Revised ICH E6: A Side-by-Side Comparison of Revisions 2 and 3

Tracking the Revised ICH E6: A Side-by-Side Comparison of Revisions 2 and 3

$275.00
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GCP Questions, FDA Answers 2023 Edition

GCP Questions, FDA Answers, 2023 Edition

$397.00
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Best Practices for Clinical Trial Site Management, Volume 3

Best Practices for Clinical Trial Site Management, Vol. 3

$159.00
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International Standards for Clinical Trials

International Standards for Clinical Trials: Manual of ICH Efficacy Guidelines

$249.00
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Clinical Data Integrity - cover

Clinical Data Integrity: FDA and DOJ Enforcement Priorities

$129.00
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Clinical Trials Adverse Event Reporting Guide, 2022 Edition cover

Clinical Trials Adverse Event Reporting Guide, 2022 Edition

$249.00
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The Investigator’s Guide to Form FDA 1572

The Investigator’s Guide to Form FDA 1572: Getting the Statement of Investigator Right

$149.00
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GCP Questions, FDA Answers, 2022 Edition

GCP Questions, FDA Answers, 2022 Edition

$397.00
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Safety Reporting Overload in Clinical Trials

Safety Reporting Overload in Clinical Trials: FDA and Site Perspectives on Overreporting of Adverse Events

$129.00
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Best Practices 2

Best Practices for Clinical Trial Site Management, Vol. 2

$129.00
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Avoiding Inspection Pitfalls: Understanding Common FDA and EMA Observations

Avoiding Inspection Pitfalls: Understanding Common FDA and EMA Observations

$129.00
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The EU’s New Clinical Trial Regulation: How Sites and Sponsors Can Prepare for the Change

The EU’s New Clinical Trial Regulation: How Sites and Sponsors Can Prepare for the Change

$229.00
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